A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185169



Internal ID20752209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33577701..33580400hg38UCSC Ensembl
chr18:31157665..31160364hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523880
Supporting Variants
Samples
Known GenesASXL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185169
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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