A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988158



Internal ID18870066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:45111223..45111409hg38UCSC Ensembl
Outerchr11:45132774..45132960hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133260
Supporting Variants
SamplesKWS1
Known GenesPRDM11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988158
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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