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dbVar

Database of genomic structural variation

nsv5925583

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:323

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: 143 SVs from 49 studies. See in: genome view

Submitted genomic69,238,354-69,238,676

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5925583	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	69,238,354	69,238,676
nsv5925583	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	70,998,110	70,998,432

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17354110	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17354110	Submitted genomic		NC_000010.11:g.692 38354_69238676del	GRCh38 (hg38)		NC_000010.11	Chr10	69,238,354	69,238,676
nssv17354110	Remapped	Perfect	NC_000010.10:g.709 98110_70998432del	GRCh37.p13	First Pass	NC_000010.10	Chr10	70,998,110	70,998,432

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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