A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455327



Internal ID233408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35221605..35303036hg38UCSC Ensembl
chr5:35221707..35303138hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3881432
hg1981432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964250
Samples
Known GenesPRLR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455327
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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