A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656310



Internal ID15392962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:133029797..133138494hg38UCSC Ensembl
Innerchr6:133350936..133459633hg19UCSC Ensembl
Innerchr6:133392629..133501326hg18UCSC Ensembl
Innerchr6:133392629..133501326hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38108698
hg19108698
hg18108698
hg17108698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519475
Supporting Variants
Samples
Known GenesLINC00326
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656310
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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