A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534076



Internal ID20907437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47278011..47278781hg38UCSC Ensembl
chr18:44804382..44805152hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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