A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990761



Internal ID21900104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95159633..95159687hg38UCSC Ensembl
chr2:95825378..95825432hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990761
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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