A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154755



Internal ID22085260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88746433..88781692hg38UCSC Ensembl
Outerchr11:88743023..88786327hg38UCSC Ensembl
Innerchr11:88479601..88514860hg19UCSC Ensembl
Outerchr11:88476191..88519495hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3843305
hg1943305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007234
Samples
Known GenesGRM5
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154755
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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