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dbVar

Database of genomic structural variation

nsv6111684

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Wu et al. 2021

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: 217 SVs from 18 studies. See in: genome view

Submitted genomic54,200,195-54,200,195

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6111684	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	54,200,195	54,200,195
nsv6111684	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	51,726,565	51,726,565

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17626790	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17626790	Submitted genomic		NC_000018.10:g.542 00195_54200196ins3 11	GRCh38 (hg38)		NC_000018.10	Chr18	54,200,195	54,200,195
nssv17626790	Remapped	Perfect	NC_000018.9:g.5172 6565_51726566ins31 1	GRCh37.p13	First Pass	NC_000018.9	Chr18	51,726,565	51,726,565

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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