A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436480



Internal ID215095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63489191..63489246hg38UCSC Ensembl
chr2:63716325..63716380hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16914934
Samples
Known GenesWDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436480
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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