A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178820



Internal ID20745860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31958772..31968648hg38UCSC Ensembl
chr18:29538735..29548611hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg389877
hg199877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178820
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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