A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521359



Internal ID20894720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44715283..44715594hg38UCSC Ensembl
chr18:42295248..42295559hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041193
Samples
Known GenesSETBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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