A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518636



Internal ID20891997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33863319..33875029hg38UCSC Ensembl
chr18:31443283..31454993hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3811711
hg1911711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041294
Samples
Known GenesNOL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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