A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532138



Internal ID20905499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39705535..39705848hg38UCSC Ensembl
chr18:37285499..37285812hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040193
Samples
Known GenesLINC00669
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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