A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460162



Internal ID238156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68432043..68440204hg38UCSC Ensembl
chr5:67727870..67736031hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg388162
hg198162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460162
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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