A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981669



Internal ID21891012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165695568..165695644hg38UCSC Ensembl
chr1:165664805..165664881hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536421
Samples
Known GenesALDH9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981669
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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