A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954743



Internal ID22729978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61593490..61631313hg38UCSC Ensembl
chr20:60168546..60206369hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3837824
hg1937824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397018
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954743
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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