A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516792



Internal ID20890153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:1973023..2097943hg38UCSC Ensembl
chr18:1973024..2097944hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38124921
hg19124921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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