A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523961



Internal ID8418236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20063000..20090680hg38UCSC Ensembl
Innerchr13:20637140..20664819hg19UCSC Ensembl
Innerchr13:19535140..19562819hg18UCSC Ensembl
Innerchr13:19535140..19562819hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3827681
hg1927680
hg1827680
hg1727680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699811
Samples
Known GenesZMYM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523961
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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