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dbVar

Database of genomic structural variation

nsv6247960

Organism: Homo sapiens

Study:nstd215 (Prakrithi et al. 2022)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Prakrithi et al. 2022

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 103 SVs from 28 studies. See in: genome view

Submitted genomic33,653,951-33,653,951

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6247960	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	33,653,951	33,653,951
nsv6247960	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	33,675,497	33,675,497

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17844474	alu insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17844474	Submitted genomic		NC_000011.10:g.336 53951_33653952ins2 75	GRCh38 (hg38)		NC_000011.10	Chr11	33,653,951	33,653,951
nssv17844474	Remapped	Perfect	NC_000011.9:g.3367 5497_33675498ins27 5	GRCh37.p13	First Pass	NC_000011.9	Chr11	33,675,497	33,675,497

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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