A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472626



Internal ID250331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76524839..76532241hg38UCSC Ensembl
chr4:77445992..77453394hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg387403
hg197403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952350
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472626
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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