A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981126



Internal ID21890469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149893036..149893163hg38UCSC Ensembl
chr1:149864590..149864717hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981126
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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