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dbVar

Database of genomic structural variation

nsv6095977

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: 106 SVs from 28 studies. See in: genome view

Submitted genomic52,558,276-52,558,276

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6095977	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	52,558,276	52,558,276
nsv6095977	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	52,592,188	52,592,188

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17635751	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17635751	Submitted genomic		NC_000016.10:g.525 58276_52558277ins1 99	GRCh38 (hg38)		NC_000016.10	Chr16	52,558,276	52,558,276
nssv17635751	Remapped	Perfect	NC_000016.9:g.5259 2188_52592189ins19 9	GRCh37.p13	First Pass	NC_000016.9	Chr16	52,592,188	52,592,188

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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