A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134156



Internal ID19252598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:75153116..75153190hg38UCSC Ensembl
Outerchr11:74864161..74864235hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970499
SamplesKWS2
Known GenesSLCO2B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134156
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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