A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958946



Internal ID18875503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:133449505..133453005hg38UCSC Ensembl
Outerchr11:133319400..133322900hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118440
Supporting Variants
SamplesKWS1
Known GenesOPCML
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958946
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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