A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002216



Internal ID19091433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162153428..162237872hg38UCSC Ensembl
Innerchr3:161871216..161955660hg19UCSC Ensembl
Innerchr3:163353910..163438354hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3884445
hg1984445
hg1884445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4932n100
Supporting Variantsnssv3741567, nssv3607920, nssv3741566, nssv3607919, nssv3607921, nssv3607922
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)nsv1002216
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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