A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153277



Internal ID15526122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:299506..438449hg38UCSC Ensembl
Innerchr5:299621..438564hg19UCSC Ensembl
Innerchr5:352621..491564hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38138944
hg19138944
hg18138944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596614
Supporting Variants
SamplesHGDP00045
Known GenesAHRR, PDCD6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153277
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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