A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv772n145



Internal ID22813788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88658829..88666750hg38UCSC Ensembl
chr3:88707979..88715900hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg387922
hg197922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112665, nsv3113653
Samplessample280, sample142, sample52
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv772n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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