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dbVar

Database of genomic structural variation

nsv5961998

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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: 102 SVs from 21 studies. See in: genome view

Submitted genomic134,811,242-134,811,242

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961998	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	134,811,242	134,811,242
nsv5961998	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	134,530,084	134,530,084

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17406258	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17406258	Submitted genomic		NC_000003.12:g.134 811242_134811243in s179	GRCh38 (hg38)		NC_000003.12	Chr3	134,811,242	134,811,242
nssv17406258	Remapped	Perfect	NC_000003.11:g.134 530084_134530085in s179	GRCh37.p13	First Pass	NC_000003.11	Chr3	134,530,084	134,530,084

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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