A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511675



Internal ID20885005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89527682..89572709hg38UCSC Ensembl
chr15:90070913..90115940hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3845028
hg1945028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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