A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv992702



Internal ID15939972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68575796..68624885hg38UCSC Ensembl
Innerchr4:69441514..69490603hg19UCSC Ensembl
Innerchr4:69124109..69173198hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3849090
hg1949090
hg1849090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594557
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)nssv992702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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