A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972743



Internal ID18607959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63010451..63110185hg38UCSC Ensembl
Innerchr9:66915423..67015157hg19UCSC Ensembl
Innerchr9:66655243..66754977hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3899735
hg1999735
hg1899735
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2548063, nssv2548062, nssv2548058, nssv2548057, nssv2548064, nssv2548065, nssv2548060, nssv2548061, nssv2548059, nssv2548056
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)nsv972743
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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