A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528600



Internal ID304652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32657999..32707324hg38UCSC Ensembl
chr20:31245801..31295126hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3849326
hg1949326
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731966
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528600
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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