A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022532



Internal ID21931875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95544203..95546280hg38UCSC Ensembl
chr15:96087432..96089509hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022532
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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