A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026044



Internal ID21935387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63327624..63332770hg38UCSC Ensembl
chr15:63619823..63624969hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg385147
hg195147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601633
Samples
Known GenesCA12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026044
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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