A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449792



Internal ID228019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53971133..53978213hg38UCSC Ensembl
chr2:54198270..54205350hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg387081
hg197081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16913111
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449792
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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