A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521111



Internal ID20894472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76768168..76781140hg38UCSC Ensembl
chr18:74480124..74493096hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3812973
hg1912973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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