A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997394



Internal ID19156932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99210576..99232120hg38UCSC Ensembl
Innerchr3:98929420..98950964hg19UCSC Ensembl
Innerchr3:100412110..100433654hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3821545
hg1921545
hg1821545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4823n100
Supporting Variantsnssv3603458, nssv3603459, nssv3603455, nssv3603457, nssv3603456
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)nsv997394
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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