A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982299



Internal ID18617494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65670621..65717292hg38UCSC Ensembl
Innerchr9:70448753..70495424hg19UCSC Ensembl
Innerchr9:69688573..69735244hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3846672
hg1946672
hg1846672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2551451, nssv2551454, nssv2551456, nssv2551455, nssv2551452, nssv2551457, nssv2551450, nssv2551458, nssv2551449, nssv2551453
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD3, CBWD5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982299
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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