A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533017



Internal ID20906378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73055501..73058500hg38UCSC Ensembl
chr18:70722736..70725735hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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