A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975384



Internal ID18610592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121196829..121203991hg38UCSC Ensembl
Innerchr11:121067538..121074700hg19UCSC Ensembl
Innerchr11:120572748..120579910hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg387163
hg197163
hg187163
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764835
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975384
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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