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dbVar

Database of genomic structural variation

nsv5657103

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: 288 SVs from 32 studies. See in: genome view

Submitted genomic1,629,072-1,629,072

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657103	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	1,629,072	1,629,072
nsv5657103	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	1,629,071	1,629,071

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103249	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
nssv17103249	Submitted genomic		NC_000019.10:g.162 9072_1629073ins71	GRCh38 (hg38)		NC_000019.10	Chr19	1,629,072	1,629,072
nssv17103249	Remapped	Perfect	NC_000019.9:g.1629 071_1629072ins71	GRCh37.p13	First Pass	NC_000019.9	Chr19	1,629,071	1,629,071

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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