A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505327



Internal ID20878595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77579233..77598997hg38UCSC Ensembl
chr15:77871575..77891339hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3819765
hg1919765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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