A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134178



Internal ID18926791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:115414722..115414774hg38UCSC Ensembl
Outerchr11:115285440..115285492hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971660, nssv3983217
SamplesKWS1, KWS2
Known GenesCADM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134178
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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