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dbVar

Database of genomic structural variation

nsv5937711

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:53

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: 159 SVs from 28 studies. See in: genome view

Submitted genomic60,298,088-60,298,140

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5937711	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	60,298,088	60,298,140
nsv5937711	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	58,375,449	58,375,501

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17388091	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17388091	Submitted genomic		NC_000017.11:g.602 98088_60298140del	GRCh38 (hg38)		NC_000017.11	Chr17	60,298,088	60,298,140
nssv17388091	Remapped	Perfect	NC_000017.10:g.583 75449_58375501del	GRCh37.p13	First Pass	NC_000017.10	Chr17	58,375,449	58,375,501

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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