A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508665



Internal ID20881969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63554371..63555007hg38UCSC Ensembl
chr15:63846570..63847206hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025635
Samples
Known GenesUSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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