Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

Please click here to confirm download.

Supporting Variant Placements for estd210
Study ID	Variant ID	Variant Region type	Variant Call type	Sampleset ID	Method	Analysis ID	Validation	Variant samples	Subject phenotype	Clinical Interpretation	Assembly	Accession	Chr	Outer-Start	Start	Inner-Start	Inner-End	End	Outer-End	Placement Type	Remap Score
estd210	essv26058942		interchromosomal translocation		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh37 (hg19)	NC_000002.11	2		8181790			8181790		Submitted genomic
estd210	essv26058942		interchromosomal translocation		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh37 (hg19)	NC_000007.13	7		135245984			135245984		Submitted genomic
estd210	essv26058942		interchromosomal translocation		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh37 (hg19)	NC_000002.11	2		8181790			8181790		Submitted genomic
estd210	essv26058942		interchromosomal translocation		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh37 (hg19)	NC_000007.13	7		135245984			135245984		Submitted genomic
estd210	essv26058942		interchromosomal translocation		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh38.p12	NC_000002.12	2		8041660			8041660		Remapped	1
estd210	essv26058942		interchromosomal translocation		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh38.p12	NC_000007.14	7		135561236			135561236		Remapped	1
estd210	essv26058943		inversion		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh37 (hg19)	NC_000002.11	2		22350265			162196595		Submitted genomic
estd210	essv26058943		inversion		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh37 (hg19)	NC_000002.11	2		22350265			162196595		Submitted genomic
estd210	essv26058943		inversion		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1			GRCh38.p12	NC_000002.12	2		22127393			161340084		Remapped	0.99547
estd210	essv26058944		inversion		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1	mental retardation, neurodevelopmental disorder		GRCh37 (hg19)	NC_000002.11	2		185679985			188161779		Submitted genomic
estd210	essv26058944		inversion		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1	mental retardation, neurodevelopmental disorder		GRCh37 (hg19)	NC_000002.11	2		185679985			188161779		Submitted genomic
estd210	essv26058944		inversion		Sequencing	Split read and paired-end mapping	Yes	10001047_1_1	mental retardation, neurodevelopmental disorder		GRCh38.p12	NC_000002.12	2		184815258			187297052		Remapped	1
estd210	essv26058945		deletion		Sequencing	Split read and paired-end mapping	No	10001047_1_1			GRCh37 (hg19)	NC_000019.9	19		54800252			54809071		Submitted genomic
estd210	essv26058945		deletion		Sequencing	Split read and paired-end mapping	No	10001047_1_1			GRCh37 (hg19)	NC_000019.9	19		54800252			54809071		Submitted genomic
estd210	essv26058945		deletion		Sequencing	Split read and paired-end mapping	No	10001047_1_1			GRCh38.p12	NT_187693.1	19\|NT_187693.1		271366			280185		Remapped	1
estd210	essv26058945		deletion		Sequencing	Split read and paired-end mapping	No	10001047_1_1			GRCh38.p12	NW_003571054.1	19\|NW_003571054.1		271137			279956		Remapped	1
estd210	essv26058945		deletion		Sequencing	Split read and paired-end mapping	No	10001047_1_1			GRCh38.p12	NW_003571055.2	19\|NW_003571055.2		271018			279838		Remapped	1.00011
estd210	essv26058945		deletion		Sequencing	Split read and paired-end mapping	No	10001047_1_1			GRCh38.p12	NW_003571061.2	19\|NW_003571061.2		271393			280212		Remapped	1

You are here: NCBI