A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965297



Internal ID18862740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:133449602..133452999hg38UCSC Ensembl
Outerchr11:133319497..133322894hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383398
hg193398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121304
Supporting Variants
SamplesKWS1
Known GenesOPCML
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965297
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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