A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697591



Internal ID15434243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:61917439..61928292hg38UCSC Ensembl
Innerchr20:60492495..60503350hg19UCSC Ensembl
Innerchr20:59925890..59936745hg18UCSC Ensembl
Innerchr20:59925890..59936745hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810854
hg1910856
hg1810856
hg1710856
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520753
Supporting Variants
Samples
Known GenesCDH4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697591
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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