A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981099



Internal ID18877415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:55587569..55588369hg38UCSC Ensembl
Outerchr18:53254800..53255600hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118787
Supporting Variants
SamplesKWS1
Known GenesTCF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981099
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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