A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515427



Internal ID291907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61396625..61424625hg38UCSC Ensembl
chr20:59971681..59999681hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3828001
hg1928001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733482
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515427
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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