A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982311



Internal ID18617506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82426116..82438004hg38UCSC Ensembl
Innerchr9:85041031..85052919hg19UCSC Ensembl
Innerchr9:84230851..84242739hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3811889
hg1911889
hg1811889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555306, nssv2555304, nssv2555303, nssv2555307, nssv2555308, nssv2555301, nssv2555310, nssv2555302, nssv2555309, nssv2555305
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)nsv982311
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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