A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464308



Internal ID242189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92198429..92199866hg38UCSC Ensembl
chr5:91494246..91495683hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381438
hg191438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464308
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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