A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2851n106



Internal ID20162208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88760293..88760636hg38UCSC Ensembl
chr4:89681444..89681787hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135176, nsv1112073
SamplesKWS2
Known GenesFAM13A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2851n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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