A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428746



Internal ID207605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32206122..32208442hg38UCSC Ensembl
chr1:32671723..32674043hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382321
hg192321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903599
Samples
Known GenesIQCC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428746
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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