A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966720



Internal ID18894194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132943605..132944305hg38UCSC Ensembl
Outerchr11:132813500..132814200hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112613
Supporting Variants
SamplesKWS2
Known GenesOPCML
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966720
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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