A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999312



Internal ID19158848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89848661..89981728hg38UCSC Ensembl
Innerchr3:89897811..90030878hg19UCSC Ensembl
Innerchr3:89980501..90113568hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38133068
hg19133068
hg18133068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4810n100
Supporting Variantsnssv3603278
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)nsv999312
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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