A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467650



Internal ID245460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83063275..83063803hg38UCSC Ensembl
chr4:83984428..83984956hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735124
Samples
Known GenesCOPS4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467650
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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