A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512892



Internal ID20886232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69871257..69960241hg38UCSC Ensembl
chr15:70163596..70252580hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3888985
hg1988985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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