A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv68n145



Internal ID22813084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119880444..119901890hg38UCSC Ensembl
chr1:120423067..120444513hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3821447
hg1921447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111701, nsv3111508
Samplessample294, sample303, sample211
Known GenesADAM30
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv68n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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