A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519330



Internal ID15099937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28283642..28303453hg38UCSC Ensembl
Innerchr17:26610668..26630479hg19UCSC Ensembl
Innerchr17:23634795..23654606hg18UCSC Ensembl
Innerchr17:23634795..23654606hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3819812
hg1919812
hg1819812
hg1719812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696795
Samples
Known GenesKRT18P55
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519330
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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