A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972694



Internal ID18607910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60829522..60845653hg38UCSC Ensembl
Innerchr9:41415794..41431925hg19UCSC Ensembl
Innerchr9:41405593..41421925hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3816132
hg1916132
hg1816333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2534594, nssv2534590, nssv2534589, nssv2534596, nssv2534598, nssv2534591, nssv2534592, nssv2534593, nssv2534595, nssv2534597
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)nsv972694
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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