A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517266



Internal ID20890627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42360434..42361100hg38UCSC Ensembl
chr18:39940399..39941065hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042070
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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