A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442689



Internal ID221109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31664000..31801000hg38UCSC Ensembl
chr2:31889069..32026069hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg38137001
hg19137001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442689
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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