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dbVar

Database of genomic structural variation

nsv6035121

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:89

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: 218 SVs from 19 studies. See in: genome view

Submitted genomic54,156,432-54,156,520

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6035121	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	54,156,432	54,156,520
nsv6035121	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	51,682,802	51,682,890

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17619585	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17619585	Submitted genomic		NC_000018.10:g.541 56432_54156520del	GRCh38 (hg38)		NC_000018.10	Chr18	54,156,432	54,156,520
nssv17619585	Remapped	Perfect	NC_000018.9:g.5168 2802_51682890del	GRCh37.p13	First Pass	NC_000018.9	Chr18	51,682,802	51,682,890

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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