A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976515



Internal ID18265035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:111520053..111527125hg38UCSC Ensembl
Innerchr11:111390778..111397850hg19UCSC Ensembl
Innerchr11:110895988..110903060hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg387073
hg197073
hg187073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2766454
SamplesHGDP00542
Known GenesC11orf88
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976515
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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