A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528807



Internal ID15109414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31025813..31032220hg38UCSC Ensembl
Innerchr6:30993590..30999997hg19UCSC Ensembl
Innerchr6:31101569..31107976hg18UCSC Ensembl
Innerchr6:31101569..31107976hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg386408
hg196408
hg186408
hg176408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705481
Samples
Known GenesMUC22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528807
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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