A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989007



Internal ID18885891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132688692..132688981hg38UCSC Ensembl
Outerchr11:132558587..132558876hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135446
Supporting Variants
SamplesKWS2
Known GenesOPCML
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989007
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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