A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1038110



Internal ID15544610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95639888..95652778hg38UCSC Ensembl
Innerchr5:94975592..94988482hg19UCSC Ensembl
Innerchr5:95001348..95014238hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3812891
hg1912891
hg1812891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598960
Supporting Variants
Samples
Known GenesRFESD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1038110
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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