A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567739



Internal ID18866020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66740464..66782825hg38UCSC Ensembl
Innerchr17:64736582..64778943hg19UCSC Ensembl
Innerchr17:62167044..62209405hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3842362
hg1942362
hg1842362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056581
Supporting Variants
Samples
Known GenesPRKCA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567739
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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