A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045196



Internal ID21954466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61425779..61425901hg38UCSC Ensembl
chr20:60000835..60000957hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631743
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045196
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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