A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427867



Internal ID206759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73492157..73492265hg38UCSC Ensembl
chr1:73957840..73957948hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427867
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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