A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968737



Internal ID18257279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96499186..96503444hg38UCSC Ensembl
Innerchr9:99261468..99265726hg19UCSC Ensembl
Innerchr9:98301289..98305547hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384259
hg194259
hg184259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2560268, nssv2560273, nssv2560269, nssv2560276, nssv2560277, nssv2560272, nssv2560274, nssv2560275, nssv2560270, nssv2560271
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCDC14B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968737
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer