A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575894



Internal ID16016617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66381708..66408004hg38UCSC Ensembl
Innerchr17:64377826..64404122hg19UCSC Ensembl
Innerchr17:61808288..61834584hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3826297
hg1926297
hg1826297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875848
Samples
Known GenesPRKCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575894
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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