A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6332n223



Internal ID22809300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98147620..98150206hg38UCSC Ensembl
chr6:98595496..98598082hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg382587
hg192587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6600349, nsv6606097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6332n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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