A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522880



Internal ID15450173
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698536
Samples
Known GenesBIRC7, FLJ16779, NKAIN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522880
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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