A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987529



Internal ID21896872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212763555..212763631hg38UCSC Ensembl
chr2:213628279..213628355hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987529
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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