A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985564



Internal ID21894907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113050925..113051008hg38UCSC Ensembl
chr2:113808502..113808585hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519846
Samples
Known GenesIL36B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985564
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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