A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458665



Internal ID236685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77794306..77795107hg38UCSC Ensembl
chr5:77090130..77090931hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458665
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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