A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982999



Internal ID18618193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30367407..30373331hg38UCSC Ensembl
Innerchr11:30388954..30394878hg19UCSC Ensembl
Innerchr11:30345530..30351454hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg385925
hg195925
hg185925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1880034, nssv1880035, nssv1880033, nssv1880029, nssv1880038, nssv1880031, nssv1880030, nssv1880037, nssv1880036, nssv1880032
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)nsv982999
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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