A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974841



Internal ID18263364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87911161..87915039hg38UCSC Ensembl
Innerchr16:87944767..87948645hg19UCSC Ensembl
Innerchr16:86502268..86506146hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383879
hg193879
hg183879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2069660, nssv2069665, nssv2069664, nssv2069659, nssv2069658, nssv2069656, nssv2069657, nssv2069661, nssv2069662, nssv2069663
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCA5A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974841
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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