A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972810



Internal ID18261340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133009500..133022589hg38UCSC Ensembl
Innerchr9:135884887..135897976hg19UCSC Ensembl
Innerchr9:134874708..134887797hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3813090
hg1913090
hg1813090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2566944, nssv2566942, nssv2566941, nssv2566939, nssv2566938, nssv2566943, nssv2566936, nssv2566937, nssv2566940, nssv2566935
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)nsv972810
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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