A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453539



Internal ID231659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203026615..203033314hg38UCSC Ensembl
chr2:203891338..203898037hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924355
Samples
Known GenesNBEAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453539
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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