A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520772



Internal ID20894133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78810725..78814614hg38UCSC Ensembl
chr18:76570725..76574614hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg383890
hg193890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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