A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983013



Internal ID21892356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235173754..235173815hg38UCSC Ensembl
chr1:235337069..235337130hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533074
Samples
Known GenesARID4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983013
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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