A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057554



Internal ID21966787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41555133..41555263hg38UCSC Ensembl
chr20:40183772..40183902hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623624
Samples
Known GenesCHD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057554
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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