A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427805



Internal ID206699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109248519..109248624hg38UCSC Ensembl
chr1:109791141..109791246hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427805
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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