A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981961



Internal ID21891304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182383480..182384888hg38UCSC Ensembl
chr1:182352615..182354023hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381409
hg191409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535770
Samples
Known GenesGLUL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981961
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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