A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567735



Internal ID18866016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66508526..66596459hg38UCSC Ensembl
Innerchr17:64504644..64592577hg19UCSC Ensembl
Innerchr17:61935106..62023039hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3887934
hg1987934
hg1887934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058004
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)nssv3567735
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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