A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972413



Internal ID18607629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87771928..87773223hg38UCSC Ensembl
Innerchr9:90386843..90388138hg19UCSC Ensembl
Innerchr9:89576663..89577958hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381296
hg191296
hg181296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2556400, nssv2556403, nssv2556397, nssv2556399, nssv2556402, nssv2556398, nssv2556405, nssv2556401, nssv2556396, nssv2556404
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCTSL3P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972413
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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