A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014661



Internal ID18757196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8783669..8814814hg38UCSC Ensembl
Innerchr3:8825355..8856500hg19UCSC Ensembl
Innerchr3:8800355..8831500hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3831146
hg1931146
hg1831146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4678n100
Supporting Variantsnssv3591861
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)nsv1014661
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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