A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990656



Internal ID21899999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95046834..95046919hg38UCSC Ensembl
chr2:95712579..95712664hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535059
Samples
Known GenesMAL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990656
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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