A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437668



Internal ID216252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15024690..15348473hg38UCSC Ensembl
chr2:15164814..15488597hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38323784
hg19323784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910108
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437668
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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