A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525175



Internal ID15452468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56440110..56450706hg38UCSC Ensembl
Innerchr20:55015166..55025762hg19UCSC Ensembl
Innerchr20:54448573..54459169hg18UCSC Ensembl
Innerchr20:54448573..54459169hg17UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3810597
hg1910597
hg1810597
hg1710597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701251
Samples
Known GenesCASS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525175
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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