A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510189



Internal ID20883506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80237434..80256440hg38UCSC Ensembl
chr15:80529776..80548782hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3819007
hg1919007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189107
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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