A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656255



Internal ID15392907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85879572..85939987hg38UCSC Ensembl
Innerchr6:86589290..86649705hg19UCSC Ensembl
Innerchr6:86646009..86706424hg18UCSC Ensembl
Innerchr6:86646009..86706424hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3860416
hg1960416
hg1860416
hg1760416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519457
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656255
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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