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dbVar

Database of genomic structural variation

nsv5935436

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:50

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

Submitted genomic21,016,078-21,016,127

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5935436	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	21,016,078	21,016,127
nsv5935436	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	20,919,391	20,919,440

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17372036	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17372036	Submitted genomic		NC_000017.11:g.210 16078_21016127del	GRCh38 (hg38)		NC_000017.11	Chr17	21,016,078	21,016,127
nssv17372036	Remapped	Perfect	NC_000017.10:g.209 19391_20919440del	GRCh37.p13	First Pass	NC_000017.10	Chr17	20,919,391	20,919,440

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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