A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669785



Internal ID15059751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21811368..21874505hg38UCSC Ensembl
Innerchr1:22137861..22200998hg19UCSC Ensembl
Innerchr1:22010448..22073585hg18UCSC Ensembl
Innerchr1:21883167..21946304hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3863138
hg1963138
hg1863138
hg1763138
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515659
Supporting Variants
Samples
Known GenesHSPG2, LDLRAD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669785
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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