A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv968104



Internal ID15915374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96813383..96814977hg38UCSC Ensembl
Innerchr3:96532227..96533821hg19UCSC Ensembl
Innerchr3:98014917..98016511hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381595
hg191595
hg181595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591039
Supporting Variants
Samples
Known GenesEPHA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv968104
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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