A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972052



Internal ID18607268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83329074..83330936hg38UCSC Ensembl
Innerchr11:83040117..83041979hg19UCSC Ensembl
Innerchr11:82717765..82719627hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381863
hg191863
hg181863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1897792, nssv1897785, nssv1897787, nssv1897784, nssv1897791, nssv1897793, nssv1897789, nssv1897790, nssv1897788, nssv1897786
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)nsv972052
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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