A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3796n223



Internal ID22806764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15217101..15225200hg38UCSC Ensembl
chr2:15357225..15365324hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6352886, nsv6354575
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3796n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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