A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190574



Internal ID20757614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32555239..32583174hg38UCSC Ensembl
chr18:30135202..30163137hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3827936
hg1927936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530418
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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