A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989091



Internal ID18869999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125183242..125183484hg38UCSC Ensembl
Outerchr11:125053138..125053380hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135527
Supporting Variants
SamplesKWS1
Known GenesPKNOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989091
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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