A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012637



Internal ID18755169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4079539..4172280hg38UCSC Ensembl
Innerchr3:4121223..4213964hg19UCSC Ensembl
Innerchr3:4096223..4188964hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3892742
hg1992742
hg1892742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4648n100
Supporting Variantsnssv3590457
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)nsv1012637
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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