A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014700



Internal ID18757235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..110923hg38UCSC Ensembl
Innerchr3:60333..152606hg19UCSC Ensembl
Innerchr3:35333..127606hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3892269
hg1992274
hg1892274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590198, nssv3590197
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)nsv1014700
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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