A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018251



Internal ID21927594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21851356..21851446hg38UCSC Ensembl
chr6:21851587..21851677hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558498
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018251
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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