A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982498



Internal ID18617693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67914326..67919820hg38UCSC Ensembl
Innerchr9:67981772..67987266hg19UCSC Ensembl
Innerchr9:67571592..67577086hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385495
hg195495
hg185495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv92n82
Supporting Variantsnssv2742704, nssv2742702, nssv2742705, nssv2742703, nssv2742707, nssv2742699, nssv2742698, nssv2742701, nssv2742706, nssv2742700
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982498
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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