A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985456



Internal ID21894799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113979318..113979376hg38UCSC Ensembl
chr2:114736895..114736953hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534223
Samples
Known GenesLOC100499194
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985456
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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