A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121828



Internal ID19280619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:832800..833100hg38UCSC Ensembl
Outerchr11:832800..833100hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968479
SamplesKWS2
Known GenesCD151
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121828
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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