A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv891n145



Internal ID22813907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68515998..68748292hg38UCSC Ensembl
chr4:69381716..69614010hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38232295
hg19232295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117615, nsv3117687, nsv3117272, nsv3116445, nsv3112176, nsv3111411, nsv3112864, nsv3116189, nsv3113455
Samplessample306, sample382, sample159, sample156, sample48, sample158, sample417, sample424, sample395, sample290, sample79, sample34, sample24, sample295, sample47, sample210, sample273, sample166, sample168
Known GenesUGT2B15, UGT2B17
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv891n145
Frequency
Sample Size467
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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