A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525533



Internal ID20898894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67941283..68117273hg38UCSC Ensembl
chr18:65608520..65784510hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38175991
hg19175991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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