A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972753



Internal ID18607969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65304345..65325123hg38UCSC Ensembl
Innerchr9:70197951..70218729hg19UCSC Ensembl
Innerchr9:69487771..69508873hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3820779
hg1920779
hg1821103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2550787, nssv2550792, nssv2550791, nssv2550793, nssv2550785, nssv2550786, nssv2550789, nssv2550788, nssv2550790, nssv2550784
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)nsv972753
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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