A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029365



Internal ID15882551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:43556410..43557127hg38UCSC Ensembl
Innerchr5:43556512..43557229hg19UCSC Ensembl
Innerchr5:43592269..43592986hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38718
hg19718
hg18718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597926
Supporting Variants
Samples
Known GenesPAIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1029365
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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