A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513874



Internal ID20887223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78607430..78688225hg38UCSC Ensembl
chr15:78899772..78980567hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3880796
hg1980796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182877
Samples
Known GenesCHRNA3, CHRNB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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