A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968735



Internal ID18603963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96146199..96148486hg38UCSC Ensembl
Innerchr9:98908481..98910768hg19UCSC Ensembl
Innerchr9:97948302..97950589hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382288
hg192288
hg182288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2558761, nssv2558757, nssv2558756, nssv2558755, nssv2558754, nssv2558762, nssv2558758, nssv2558759, nssv2558760, nssv2558763
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)nsv968735
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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