A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464912



Internal ID242783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73377407..73377507hg38UCSC Ensembl
chr4:74243124..74243224hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464912
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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