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dbVar

Database of genomic structural variation

nsv5659559

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: 138 SVs from 29 studies. See in: genome view

Submitted genomic14,108,729-14,108,729

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659559	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	14,108,729	14,108,729
nsv5659559	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	14,219,541	14,219,541

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103148	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17103148	Submitted genomic		NC_000019.10:g.141 08729_14108730ins3 22	GRCh38 (hg38)		NC_000019.10	Chr19	14,108,729	14,108,729
nssv17103148	Remapped	Perfect	NC_000019.9:g.1421 9541_14219542ins32 2	GRCh37.p13	First Pass	NC_000019.9	Chr19	14,219,541	14,219,541

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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