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dbVar

Database of genomic structural variation

nsv5982055

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:218,412

Publication(s):Wu et al. 2021

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: 1347 SVs from 88 studies. See in: genome view

Submitted genomic189,356,882-189,575,293

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5982055	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	189,356,882	189,575,293
nsv5982055	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	189,326,012	189,544,423

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17524822	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17524822	Submitted genomic		NC_000001.11:g.189 356882_189575293de l	GRCh38 (hg38)		NC_000001.11	Chr1	189,356,882	189,575,293
nssv17524822	Remapped	Perfect	NC_000001.10:g.189 326012_189544423de l	GRCh37.p13	First Pass	NC_000001.10	Chr1	189,326,012	189,544,423

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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