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dbVar

Database of genomic structural variation

nsv5919795

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:423

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: 176 SVs from 52 studies. See in: genome view

Submitted genomic134,665,247-134,665,669

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5919795	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	134,665,247	134,665,669
nsv5919795	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	134,349,999	134,350,421

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17437447	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17437447	Submitted genomic		NC_000007.14:g.134 665247_134665669de l	GRCh38 (hg38)		NC_000007.14	Chr7	134,665,247	134,665,669
nssv17437447	Remapped	Perfect	NC_000007.13:g.134 349999_134350421de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	134,349,999	134,350,421

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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