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dbVar

Database of genomic structural variation

nsv5626371

Organism: Homo sapiens

Study:nstd207 (Ebert 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):Ebert 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: 86 SVs from 22 studies. See in: genome view

Submitted genomic53,532,440-53,532,440

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5626371	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	53,532,440	53,532,440
nsv5626371	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	53,397,238	53,397,238

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17154836	insertion	SAMN00000419	Sequencing	Sequence alignment	1,071

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17154836	Submitted genomic		NC_000006.12:g.535 32440_53532441ins1 91	GRCh38 (hg38)		NC_000006.12	Chr6	53,532,440	53,532,440
nssv17154836	Remapped	Perfect	NC_000006.11:g.533 97238_53397239ins1 91	GRCh37.p13	First Pass	NC_000006.11	Chr6	53,397,238	53,397,238

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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