A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980874



Internal ID21890217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119879642..119902332hg38UCSC Ensembl
chr1:120422265..120444955hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3822691
hg1922691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524597
Samples
Known GenesADAM30
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980874
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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