A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428853



Internal ID207711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96925300..96929850hg38UCSC Ensembl
chr1:97390856..97395406hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg384551
hg194551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16907023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428853
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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