A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011313



Internal ID19100530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112380146..112394487hg38UCSC Ensembl
Innerchr3:112098993..112113334hg19UCSC Ensembl
Innerchr3:113581683..113596024hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3814342
hg1914342
hg1814342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4838n100
Supporting Variantsnssv3735254, nssv3604418, nssv3604419
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)nsv1011313
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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