A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516656



Internal ID20890017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73754395..74187990hg38UCSC Ensembl
chr18:71421630..71855225hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38433596
hg19433596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197185
Samples
Known GenesFBXO15, TIMM21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516656
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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