A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423884



Internal ID202892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8842362..8842937hg38UCSC Ensembl
chr1:8902421..8902996hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16889432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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