A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035139



Internal ID15888325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:76318912..76332588hg38UCSC Ensembl
Innerchr5:75614737..75628413hg19UCSC Ensembl
Innerchr5:75650493..75664169hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3813677
hg1913677
hg1813677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598678
Supporting Variants
Samples
Known GenesSV2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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