A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422600



Internal ID201641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35625835..35641835hg38UCSC Ensembl
chr1:36091436..36107436hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903691
Samples
Known GenesPSMB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422600
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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