A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699272



Internal ID15089238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85538041..85554656hg38UCSC Ensembl
Innerchr6:86247759..86264374hg19UCSC Ensembl
Innerchr6:86304478..86321093hg18UCSC Ensembl
Innerchr6:86304478..86321093hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3816616
hg1916616
hg1816616
hg1716616
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516516
Supporting Variants
Samples
Known GenesSNX14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699272
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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