A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522875



Internal ID15103482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149322573..149441401hg38UCSC Ensembl
Innerchr6:149643709..149762537hg19UCSC Ensembl
Innerchr6:149685402..149804230hg18UCSC Ensembl
Innerchr6:149685402..149804230hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38118829
hg19118829
hg18118829
hg17118829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698530
Samples
Known GenesSUMO4, TAB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522875
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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