A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982327



Internal ID18617522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97195813..97199777hg38UCSC Ensembl
Innerchr9:99958095..99962059hg19UCSC Ensembl
Innerchr9:98997916..99001880hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383965
hg193965
hg183965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561127, nssv2561132, nssv2561128, nssv2561134, nssv2561135, nssv2561133, nssv2561131, nssv2561129, nssv2561126, nssv2561130
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)nsv982327
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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