A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6418n223



Internal ID22809386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137059413..137105487hg38UCSC Ensembl
chr6:137380550..137426624hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3846075
hg1946075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6618574, nsv6608213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6418n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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