A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499295



Internal ID20872514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76930401..76933000hg38UCSC Ensembl
chr15:77222742..77225341hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185998
Samples
Known GenesRCN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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