A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526702



Internal ID15107309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:141955356..141960198hg38UCSC Ensembl
Innerchr5:141334921..141339763hg19UCSC Ensembl
Innerchr5:141315105..141319947hg18UCSC Ensembl
Innerchr5:141315105..141319947hg17UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg384843
hg194843
hg184843
hg174843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703041
Samples
Known GenesPCDH12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526702
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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