A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975164



Internal ID18610372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29725777..29731873hg38UCSC Ensembl
Innerchr11:29747324..29753420hg19UCSC Ensembl
Innerchr11:29703900..29709996hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg386097
hg196097
hg186097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1879932, nssv1879933, nssv1879936, nssv1879938, nssv1879940, nssv1879941, nssv1879935, nssv1879939, nssv1879934, nssv1879937
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)nsv975164
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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