A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029372



Internal ID15882558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:43556595..43557303hg38UCSC Ensembl
Innerchr5:43556697..43557405hg19UCSC Ensembl
Innerchr5:43592454..43593162hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597931
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)nssv1029372
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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