A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975888



Internal ID18264409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14441379..14443544hg38UCSC Ensembl
Innerchr11:14462925..14465090hg19UCSC Ensembl
Innerchr11:14419501..14421666hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382166
hg192166
hg182166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1878619, nssv1878625, nssv1878626, nssv1878621, nssv1878617, nssv1878620, nssv1878622, nssv1878623, nssv1878624, nssv1878618
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)nsv975888
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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