A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984533



Internal ID18874604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:65572329..65572829hg38UCSC Ensembl
Outerchr11:65339800..65340300hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126297
Supporting Variants
SamplesKWS1
Known GenesFAM89B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984533
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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