A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990293



Internal ID21899636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7807832..7807888hg38UCSC Ensembl
chr2:7947963..7948019hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990293
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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