A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510534



Internal ID20883854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63591692..63595255hg38UCSC Ensembl
chr15:63883891..63887454hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383564
hg193564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025637
Samples
Known GenesUSP3, USP3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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