A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528424



Internal ID15109031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35321669..35324427hg38UCSC Ensembl
Innerchr6:35289446..35292204hg19UCSC Ensembl
Innerchr6:35397424..35400182hg18UCSC Ensembl
Innerchr6:35397424..35400182hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382759
hg192759
hg182759
hg172759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705017
Samples
Known GenesDEF6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528424
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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