A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972955



Internal ID18608171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122715968..122727889hg38UCSC Ensembl
Innerchr11:122586676..122598597hg19UCSC Ensembl
Innerchr11:122091886..122103807hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3811922
hg1911922
hg1811922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2760512
SamplesHGDP00665
Known GenesUBASH3B
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972955
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer