A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512379



Internal ID20885713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66299426..66303994hg38UCSC Ensembl
chr15:66591764..66596332hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384569
hg194569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179149
Samples
Known GenesDIS3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512379
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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