A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4128n223



Internal ID22807096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:133140126..133305633hg38UCSC Ensembl
chr2:133897698..134063205hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg38165508
hg19165508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6353373, nsv6339927
Samples
Known GenesMIR7853, NCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4128n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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