A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975137



Internal ID18610345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1191560..1200338hg38UCSC Ensembl
Innerchr11:1212760..1221564hg19UCSC Ensembl
Innerchr11:1168903..1178140hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388779
hg198805
hg189238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1872351, nssv1872350, nssv1872344, nssv1872348, nssv1872343, nssv1872342, nssv1872345, nssv1872349, nssv1872346, nssv1872347
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)nsv975137
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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