A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149790



Internal ID15532914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66414797..66475557hg38UCSC Ensembl
Innerchr17:64410915..64471675hg19UCSC Ensembl
Innerchr17:61841377..61902137hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3860761
hg1960761
hg1860761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575896
Supporting Variants
SamplesHGDP01400
Known GenesPRKCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149790
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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