A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2935n106



Internal ID20162292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166083148..166083769hg38UCSC Ensembl
chr4:167004300..167004921hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1130244, nsv1135182, nsv1121306
SamplesKWS2
Known GenesTLL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2935n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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