A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987252



Internal ID21896595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170149623..170149702hg38UCSC Ensembl
chr2:171006133..171006212hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987252
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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