A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151675



Internal ID18856381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12131061..12131318hg38UCSC Ensembl
Outerchr11:12152608..12152865hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003094
SamplesKWB1
Known GenesMICAL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151675
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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