A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429787



Internal ID208622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94605333..94610680hg38UCSC Ensembl
chr1:95070889..95076236hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg385348
hg195348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16906699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429787
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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