A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153995



Internal ID15875491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:123778493..123796185hg38UCSC Ensembl
Innerchr5:123114187..123131879hg19UCSC Ensembl
Innerchr5:123142086..123159778hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3817693
hg1917693
hg1817693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599650
Supporting Variants
SamplesHGDP00691
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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