A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692085



Internal ID15082051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92538625..94740699hg38UCSC Ensembl
Innerchr6:93248343..95450417hg19UCSC Ensembl
Innerchr6:93305064..95507138hg18UCSC Ensembl
Innerchr6:93305064..95507138hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg382202075
hg192202075
hg182202075
hg172202075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known GenesEPHA7, TSG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692085
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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