A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004170



Internal ID18746701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1373511..1720723hg38UCSC Ensembl
Innerchr3:1415195..1762407hg19UCSC Ensembl
Innerchr3:1390195..1737407hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38347213
hg19347213
hg18347213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4623n100
Supporting Variantsnssv3590311
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004170
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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