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dbVar

Database of genomic structural variation

nsv5636477

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: 186 SVs from 39 studies. See in: genome view

Submitted genomic17,650,654-17,650,654

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5636477	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	17,650,654	17,650,654
nsv5636477	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	17,650,885	17,650,885

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17143111	insertion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17143111	Submitted genomic		NC_000006.12:g.176 50654_17650655ins3 37	GRCh38 (hg38)		NC_000006.12	Chr6	17,650,654	17,650,654
nssv17143111	Remapped	Perfect	NC_000006.11:g.176 50885_17650886ins3 37	GRCh37.p13	First Pass	NC_000006.11	Chr6	17,650,885	17,650,885

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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