A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4177n223



Internal ID22807145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165679601..165701600hg38UCSC Ensembl
chr2:166536111..166558110hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3822000
hg1922000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6343399, nsv6344845
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4177n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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