A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437176



Internal ID215774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174531465..174534045hg38UCSC Ensembl
chr2:175396193..175398773hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg382581
hg192581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16921100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437176
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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