A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467849



Internal ID245659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171684724..171691260hg38UCSC Ensembl
chr5:171111728..171118264hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg386537
hg196537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467849
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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