A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3839n223



Internal ID22806807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38726101..38744100hg38UCSC Ensembl
chr2:38953243..38971242hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6342723, nsv6353822, nsv6341763
Samples
Known GenesGALM, SRSF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3839n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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