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dbVar

Database of genomic structural variation

nsv6086757

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: 104 SVs from 26 studies. See in: genome view

Submitted genomic52,577,733-52,577,733

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6086757	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	52,577,733	52,577,733
nsv6086757	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	52,611,645	52,611,645

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17620804	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17620804	Submitted genomic		NC_000016.10:g.525 77733_52577734ins1 568	GRCh38 (hg38)		NC_000016.10	Chr16	52,577,733	52,577,733
nssv17620804	Remapped	Perfect	NC_000016.9:g.5261 1645_52611646ins15 68	GRCh37.p13	First Pass	NC_000016.9	Chr16	52,611,645	52,611,645

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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