A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv44n145



Internal ID22813060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84688702..84690590hg38UCSC Ensembl
chr1:85154385..85156273hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381889
hg191889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110929, nsv3113908
Samplessample349, sample357
Known GenesSSX2IP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv44n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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