A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703869



Internal ID15440521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:42492550..42515707hg38UCSC Ensembl
Innerchr3:42534042..42557199hg19UCSC Ensembl
Innerchr3:42509046..42532203hg18UCSC Ensembl
Innerchr3:42509046..42532203hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3823158
hg1923158
hg1823158
hg1723158
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527430
Supporting Variants
Samples
Known GenesVIPR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703869
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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