A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698536



Internal ID15435188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63239113..63264557hg38UCSC Ensembl
Innerchr20:61870465..61895909hg19UCSC Ensembl
Innerchr20:61340910..61366354hg18UCSC Ensembl
Innerchr20:61340910..61366354hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3825445
hg1925445
hg1825445
hg1725445
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522880
Supporting Variants
Samples
Known GenesBIRC7, FLJ16779, NKAIN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698536
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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