A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508402



Internal ID20881702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87553175..87606572hg38UCSC Ensembl
chr15:88096406..88149803hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3853398
hg1953398
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191153
Samples
Known GenesLINC00052
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508402
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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