A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460111



Internal ID238105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168704195..168704341hg38UCSC Ensembl
chr5:168131200..168131346hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976624
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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