A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525498



Internal ID20898859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26735254..26736749hg38UCSC Ensembl
chr18:24315218..24316713hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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