A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466957



Internal ID244782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107739496..107740197hg38UCSC Ensembl
chr5:107075197..107075898hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16972235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466957
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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