A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021868



Internal ID21931211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88652408..88652473hg38UCSC Ensembl
chr15:89195639..89195704hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615972
Samples
Known GenesISG20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021868
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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