A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526935



Internal ID15454228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121539231..121554502hg38UCSC Ensembl
Innerchr6:121860377..121875648hg19UCSC Ensembl
Innerchr6:121902076..121917347hg18UCSC Ensembl
Innerchr6:121902076..121917347hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3815272
hg1915272
hg1815272
hg1715272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv394n21
Supporting Variantsnssv703303
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526935
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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