A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2832394



Internal ID15667138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41350342..41369322hg38UCSC Ensembl
Innerchr17:39506594..39525574hg19UCSC Ensembl
Innerchr17:36760120..36779100hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3818981
hg1918981
hg1818981
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514844
Supporting Variants
SamplesNA18506
Known GenesKRT33A, KRT33B
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2832394
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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