A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506199



Internal ID20879476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73499175..73515252hg38UCSC Ensembl
chr15:73791516..73807593hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3816078
hg1916078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026640
Samples
Known GenesC15orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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