A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526116



Internal ID20899477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33856301..33857100hg38UCSC Ensembl
chr18:31436265..31437064hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041293
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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