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dbVar

Database of genomic structural variation

nsv5658184

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 25 studies. See in: genome view

Submitted genomic29,957,291-29,957,291

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5658184	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	29,957,291	29,957,291
nsv5658184	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	30,448,198	30,448,198

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17104084	insertion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17104084	Submitted genomic		NC_000019.10:g.299 57291_29957292ins3 05	GRCh38 (hg38)		NC_000019.10	Chr19	29,957,291	29,957,291
nssv17104084	Remapped	Perfect	NC_000019.9:g.3044 8198_30448199ins30 5	GRCh37.p13	First Pass	NC_000019.9	Chr19	30,448,198	30,448,198

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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