A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506858



Internal ID20880144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70755482..70767401hg38UCSC Ensembl
chr15:71047821..71059740hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3811920
hg1911920
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188749
Samples
Known GenesUACA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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