A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv161n223



Internal ID22803129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38966901..38975300hg38UCSC Ensembl
chr1:39432573..39440972hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6320637, nsv6326512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv161n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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