A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7664n223



Internal ID22810632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26251601..26436800hg38UCSC Ensembl
chr9:26251599..26436798hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38185200
hg19185200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6424387, nsv6417669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7664n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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