A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983090



Internal ID21892433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234566985..234573594hg38UCSC Ensembl
chr1:234702731..234709340hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg386610
hg196610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983090
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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