A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982287



Internal ID21891630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206486431..206486568hg38UCSC Ensembl
chr1:206659768..206659905hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531310
Samples
Known GenesIKBKE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982287
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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