A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1031910



Internal ID15885096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120044817..120109366hg38UCSC Ensembl
Innerchr5:119380512..119445061hg19UCSC Ensembl
Innerchr5:119408411..119472960hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3864550
hg1964550
hg1864550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599579
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)nssv1031910
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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