A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465553



Internal ID243414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57473334..57479520hg38UCSC Ensembl
chr4:58339500..58345686hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg386187
hg196187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16949041
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465553
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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