A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000312



Internal ID18742843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4123660..4235682hg38UCSC Ensembl
Innerchr3:4165344..4277366hg19UCSC Ensembl
Innerchr3:4140344..4252366hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38112023
hg19112023
hg18112023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4654n100
Supporting Variantsnssv3590480, nssv3590479, nssv3590478
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)nsv1000312
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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