A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003136



Internal ID19092353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162148105..162235787hg38UCSC Ensembl
Innerchr3:161865893..161953575hg19UCSC Ensembl
Innerchr3:163348587..163436269hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3887683
hg1987683
hg1887683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4932n100
Supporting Variantsnssv3606430
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)nsv1003136
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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