A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591042



Internal ID16378451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:97025178..97135275hg38UCSC Ensembl
Innerchr3:96744022..96854119hg19UCSC Ensembl
Innerchr3:98226712..98336809hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38110098
hg19110098
hg18110098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv968107
Samples
Known GenesEPHA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591042
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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