A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446323



Internal ID224647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209169055..209179447hg38UCSC Ensembl
chr2:210033779..210044171hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3810393
hg1910393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446323
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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