A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012867



Internal ID18755399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2055469..2959401hg38UCSC Ensembl
Innerchr3:2097153..3001085hg19UCSC Ensembl
Innerchr3:2072153..2976085hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38903933
hg19903933
hg18903933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739544
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012867
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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