A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448732



Internal ID226994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5946186..5947372hg38UCSC Ensembl
chr2:6086318..6087504hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909877
Samples
Known GenesLINC01105
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448732
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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