A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518606



Internal ID20891967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38969530..39108741hg38UCSC Ensembl
chr18:36549494..36688705hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38139212
hg19139212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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