A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6044n223



Internal ID22809012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2567701..2573200hg38UCSC Ensembl
chr6:2567935..2573434hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6413980, nsv6412055, nsv6404261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6044n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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