A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035781



Internal ID15888967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85942022..86013760hg38UCSC Ensembl
Innerchr5:85237840..85309578hg19UCSC Ensembl
Innerchr5:85273596..85345334hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3871739
hg1971739
hg1871739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598833
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1035781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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