A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975880



Internal ID18264401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8684376..8685876hg38UCSC Ensembl
Innerchr11:8705923..8707423hg19UCSC Ensembl
Innerchr11:8662499..8663999hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381501
hg191501
hg181501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1875438, nssv1875441, nssv1875442, nssv1875445, nssv1875443, nssv1875444, nssv1875447, nssv1875446, nssv1875439, nssv1875440
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesRPL27A, SNORA45
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975880
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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