A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012735



Internal ID18755267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4104499..4166100hg38UCSC Ensembl
Innerchr3:4146183..4207784hg19UCSC Ensembl
Innerchr3:4121183..4182784hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3861602
hg1961602
hg1861602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4651n100
Supporting Variantsnssv3590467, nssv3590468
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)nsv1012735
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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