A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439782



Internal ID218313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165808971..165809188hg38UCSC Ensembl
chr2:166665481..166665698hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16921775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439782
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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