A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981689



Internal ID18874212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:134114709..134115109hg38UCSC Ensembl
Outerchr5:133450400..133450800hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145070
Supporting Variants
SamplesKWS1
Known GenesTCF7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981689
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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