A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972649



Internal ID18607865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14041094..14041685hg38UCSC Ensembl
Innerchr9:14041093..14041684hg19UCSC Ensembl
Innerchr9:14031093..14031684hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38592
hg19592
hg18592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2522079, nssv2522074, nssv2522076, nssv2522082, nssv2522078, nssv2522081, nssv2522075, nssv2522080, nssv2522077, nssv2522083
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)nsv972649
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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