A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660439



Internal ID15397091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17610934..17628680hg38UCSC Ensembl
Innerchr20:17591579..17609325hg19UCSC Ensembl
Innerchr20:17539579..17557325hg18UCSC Ensembl
Innerchr20:17539579..17557325hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3817747
hg1917747
hg1817747
hg1717747
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519542
Supporting Variants
Samples
Known GenesRRBP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660439
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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