A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982662



Internal ID21892005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226026121..226026233hg38UCSC Ensembl
chr1:226213822..226213934hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530157
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982662
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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