A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454020



Internal ID232128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160842368..161037362hg38UCSC Ensembl
chr5:160269375..160464369hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38194995
hg19194995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977418
Samples
Known GenesATP10B, LOC285629
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454020
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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