A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194957



Internal ID20761997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30962346..30973052hg38UCSC Ensembl
chr18:28542312..28553018hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3810707
hg1910707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523449
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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