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dbVar

Database of genomic structural variation

nsv6100354

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: 78 SVs from 17 studies. See in: genome view

Submitted genomic102,119,018-102,119,018

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6100354	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	102,119,018	102,119,018
nsv6100354	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	103,878,775	103,878,775

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17585581	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17585581	Submitted genomic		NC_000010.11:g.102 119018_102119019in s328	GRCh38 (hg38)		NC_000010.11	Chr10	102,119,018	102,119,018
nssv17585581	Remapped	Perfect	NC_000010.10:g.103 878775_103878776in s328	GRCh37.p13	First Pass	NC_000010.10	Chr10	103,878,775	103,878,775

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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