A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439350



Internal ID217889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240176342..240178073hg38UCSC Ensembl
chr1:240339642..240341373hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381732
hg191732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897641
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439350
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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