A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507255



Internal ID20880543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80293353..80312283hg38UCSC Ensembl
chr15:80585695..80604625hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3818931
hg1918931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188541
Samples
Known GenesLINC00927
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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