A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431566



Internal ID210339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44997585..44998247hg38UCSC Ensembl
chr1:45463257..45463919hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16904895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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