A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437062



Internal ID215661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14252581..14256473hg38UCSC Ensembl
chr4:14254205..14258097hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg383893
hg193893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437062
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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