A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984364



Internal ID18619551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88154772..88165314hg38UCSC Ensembl
Innerchr16:88188378..88198920hg19UCSC Ensembl
Innerchr16:86745879..86756421hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3810543
hg1910543
hg1810543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2070103, nssv2070098, nssv2070105, nssv2070099, nssv2070097, nssv2070100, nssv2070101, nssv2070096, nssv2070102, nssv2070104
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)nsv984364
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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