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dbVar

Database of genomic structural variation

nsv5918526

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:8,935

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: 173 SVs from 41 studies. See in: genome view

Submitted genomic103,085,711-103,094,645

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5918526	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	103,085,711	103,094,645
nsv5918526	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	102,726,158	102,735,092

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17439892	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17439892	Submitted genomic		NC_000007.14:g.103 085711_103094645de l	GRCh38 (hg38)		NC_000007.14	Chr7	103,085,711	103,094,645
nssv17439892	Remapped	Perfect	NC_000007.13:g.102 726158_102735092de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	102,726,158	102,735,092

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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