A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465116



Internal ID242987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151420014..151420720hg38UCSC Ensembl
chr5:150799575..150800281hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465116
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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