A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455599



Internal ID233677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47833581..47833728hg38UCSC Ensembl
chr4:47835598..47835745hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16949990
Samples
Known GenesCORIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455599
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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