A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499468



Internal ID20872688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39503686..39508237hg38UCSC Ensembl
chr15:39795887..39800438hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384552
hg194552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499468
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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