A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967569



Internal ID16261525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89330785..89369112hg38UCSC Ensembl
Innerchr3:89379935..89418262hg19UCSC Ensembl
Innerchr3:89462625..89500952hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3838328
hg1938328
hg1838328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590927
Supporting Variants
Samples
Known GenesEPHA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv967569
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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