A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982251



Internal ID18617446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42621793..42627891hg38UCSC Ensembl
Innerchr9:44298592..44304694hg19UCSC Ensembl
Innerchr9:44238588..44244690hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386099
hg196103
hg186103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2736218, nssv2736210, nssv2736216, nssv2736209, nssv2736215, nssv2736217, nssv2736211, nssv2736213, nssv2736212, nssv2736214
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)nsv982251
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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