A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013760



Internal ID19102979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65202778..65222043hg38UCSC Ensembl
Innerchr3:65188453..65207718hg19UCSC Ensembl
Innerchr3:65163493..65182758hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3819266
hg1919266
hg1819266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4761n100
Supporting Variantsnssv3594748, nssv3594747, nssv3594746
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013760
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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