A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502506



Internal ID20875752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65854336..65859669hg38UCSC Ensembl
chr15:66146674..66152007hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385334
hg195334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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