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dbVar

Database of genomic structural variation

nsv5655388

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: 139 SVs from 22 studies. See in: genome view

Submitted genomic76,527,197-76,527,197

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5655388	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	76,527,197	76,527,197
nsv5655388	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	74,523,279	74,523,279

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17084960	insertion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17084960	Submitted genomic		NC_000017.11:g.765 27197_76527198ins5 9	GRCh38 (hg38)		NC_000017.11	Chr17	76,527,197	76,527,197
nssv17084960	Remapped	Perfect	NC_000017.10:g.745 23279_74523280ins5 9	GRCh37.p13	First Pass	NC_000017.10	Chr17	74,523,279	74,523,279

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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