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dbVar

Database of genomic structural variation

nsv5639774

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: 91 SVs from 21 studies. See in: genome view

Submitted genomic91,260,116-91,260,116

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5639774	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	91,260,116	91,260,116
nsv5639774	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	93,019,873	93,019,873

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17072258	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17072258	Submitted genomic		NC_000010.11:g.912 60116_91260117ins6 4	GRCh38 (hg38)		NC_000010.11	Chr10	91,260,116	91,260,116
nssv17072258	Remapped	Perfect	NC_000010.10:g.930 19873_93019874ins6 4	GRCh37.p13	First Pass	NC_000010.10	Chr10	93,019,873	93,019,873

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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