A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982968



Internal ID18618162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131893..180277hg38UCSC Ensembl
Innerchr11:131893..180277hg19UCSC Ensembl
Innerchr11:121893..170277hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3848385
hg1948385
hg1848385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1871967, nssv1870394, nssv1870396, nssv1870391, nssv1870395, nssv1871966, nssv1871965, nssv1871964, nssv1870393, nssv1870392
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC01001
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982968
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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