A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434906



Internal ID213567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19376611..19385705hg38UCSC Ensembl
chr2:19576372..19585466hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg389095
hg199095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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