A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013078



Internal ID18755609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24337..127144hg38UCSC Ensembl
Innerchr3:66011..168827hg19UCSC Ensembl
Innerchr3:41011..143827hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38102808
hg19102817
hg18102817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4606n100
Supporting Variantsnssv3590228
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)nsv1013078
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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