A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997387



Internal ID18810237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..110364hg38UCSC Ensembl
Innerchr3:60333..152047hg19UCSC Ensembl
Innerchr3:35333..127047hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3891710
hg1991715
hg1891715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590196
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)nsv997387
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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