A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv160n223



Internal ID22803128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38868602..38870170hg38UCSC Ensembl
chr1:39334274..39335842hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381569
hg191569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6322141, nsv6323599
Samples
Known GenesGJA9-MYCBP, MYCBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv160n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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