A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968695



Internal ID18603923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64315968..64348610hg38UCSC Ensembl
Innerchr9:69328386..69361028hg19UCSC Ensembl
Innerchr9:68618023..68650848hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3832643
hg1932643
hg1832826
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2549383, nssv2549384, nssv2549387, nssv2549381, nssv2549385, nssv2549386, nssv2549382, nssv2549389, nssv2549388, nssv2549390
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)nsv968695
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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