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dbVar

Database of genomic structural variation

nsv5663608

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: 328 SVs from 31 studies. See in: genome view

Submitted genomic1,628,458-1,628,458

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5663608	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	1,628,458	1,628,458
nsv5663608	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	1,628,457	1,628,457

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103239	insertion	NA12329	Sequencing	Sequence alignment	1,517

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17103239	Submitted genomic		NC_000019.10:g.162 8458_1628459ins536	GRCh38 (hg38)		NC_000019.10	Chr19	1,628,458	1,628,458
nssv17103239	Remapped	Perfect	NC_000019.9:g.1628 457_1628458ins536	GRCh37.p13	First Pass	NC_000019.9	Chr19	1,628,457	1,628,457

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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