A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1038089



Internal ID15891275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93584115..93584954hg38UCSC Ensembl
Innerchr5:92919821..92920660hg19UCSC Ensembl
Innerchr5:92945577..92946416hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598944
Supporting Variants
Samples
Known GenesNR2F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1038089
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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