A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527528



Internal ID15454821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158903519..158903940hg38UCSC Ensembl
Innerchr6:159324551..159324972hg19UCSC Ensembl
Innerchr6:159244539..159244960hg18UCSC Ensembl
Innerchr6:159294960..159295381hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38422
hg19422
hg18422
hg17422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703986
Samples
Known GenesC6orf99
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527528
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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