A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463907



Internal ID241797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:31533389..31533458hg38UCSC Ensembl
chr5:31533496..31533565hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964106
Samples
Known GenesC5orf22
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463907
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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