A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985502



Internal ID21894845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102869504..102874281hg38UCSC Ensembl
chr2:103485963..103490740hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg384778
hg194778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985502
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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