A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515713



Internal ID20889074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45974953..45982564hg38UCSC Ensembl
chr18:43554919..43562530hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg387612
hg197612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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