A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522792



Internal ID20896153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28352901..28363400hg38UCSC Ensembl
chr18:25932865..25943364hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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