A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984367



Internal ID18619554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:90083106..90097467hg38UCSC Ensembl
Innerchr16:90149514..90163875hg19UCSC Ensembl
Innerchr16:88677015..88691376hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3814362
hg1914362
hg1814362
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2071245, nssv2071246, nssv2071242, nssv2071239, nssv2071241, nssv2071237, nssv2071240, nssv2071238, nssv2071244, nssv2071243
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984367
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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