A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153299



Internal ID15877020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28792606..28841838hg38UCSC Ensembl
Innerchr5:28792713..28841945hg19UCSC Ensembl
Innerchr5:28828470..28877702hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3849233
hg1949233
hg1849233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597718
Supporting Variants
SamplesHGDP00926
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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