A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702721



Internal ID15092687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123307142..123576152hg38UCSC Ensembl
Innerchr6:123628287..123897297hg19UCSC Ensembl
Innerchr6:123669986..123938996hg18UCSC Ensembl
Innerchr6:123669986..123938996hg17UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38269011
hg19269011
hg18269011
hg17269011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526420
Supporting Variants
Samples
Known GenesTRDN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702721
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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