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dbVar

Database of genomic structural variation

nsv5659438

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: 326 SVs from 33 studies. See in: genome view

Submitted genomic1,627,976-1,627,976

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659438	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	1,627,976	1,627,976
nsv5659438	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	1,627,975	1,627,975

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103232	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17103232	Submitted genomic		NC_000019.10:g.162 7976_1627977ins104	GRCh38 (hg38)		NC_000019.10	Chr19	1,627,976	1,627,976
nssv17103232	Remapped	Perfect	NC_000019.9:g.1627 975_1627976ins104	GRCh37.p13	First Pass	NC_000019.9	Chr19	1,627,975	1,627,975

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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