A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520787



Internal ID20894148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27774264..27803225hg38UCSC Ensembl
chr18:25354228..25383189hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3828962
hg1928962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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