A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982451



Internal ID21891794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212126815..212127000hg38UCSC Ensembl
chr1:212300157..212300342hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982451
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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