A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526542



Internal ID15107149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66292519..66307675hg38UCSC Ensembl
Innerchr17:64288637..64303793hg19UCSC Ensembl
Innerchr17:61719099..61734255hg18UCSC Ensembl
Innerchr17:61719099..61734255hg17UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3815157
hg1915157
hg1815157
hg1715157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702856
Samples
Known GenesPRKCA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526542
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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