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dbVar

Database of genomic structural variation

nsv5614091

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: 107 SVs from 23 studies. See in: genome view

Submitted genomic134,701,277-134,701,277

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5614091	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	134,701,277	134,701,277
nsv5614091	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	134,420,119	134,420,119

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17134689	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
nssv17134689	Submitted genomic		NC_000003.12:g.134 701277_134701278in s75	GRCh38 (hg38)		NC_000003.12	Chr3	134,701,277	134,701,277
nssv17134689	Remapped	Perfect	NC_000003.11:g.134 420119_134420120in s75	GRCh37.p13	First Pass	NC_000003.11	Chr3	134,420,119	134,420,119

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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