A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704319



Internal ID15440971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68525208..68532062hg38UCSC Ensembl
Innerchr6:69235100..69241954hg19UCSC Ensembl
Innerchr6:69291821..69298675hg18UCSC Ensembl
Innerchr6:69291821..69298675hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg386855
hg196855
hg186855
hg176855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515885
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704319
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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