A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1038087



Internal ID15891273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93584115..93584720hg38UCSC Ensembl
Innerchr5:92919821..92920426hg19UCSC Ensembl
Innerchr5:92945577..92946182hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38606
hg19606
hg18606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598943
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)nssv1038087
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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