A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498770



Internal ID20871983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39500690..39510431hg38UCSC Ensembl
chr15:39792891..39802632hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389742
hg199742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498770
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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