A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420816



Internal ID199909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25045089..25047805hg38UCSC Ensembl
chr1:25371580..25374296hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382717
hg192717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420816
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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