A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190067



Internal ID20757107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32000694..32006204hg38UCSC Ensembl
chr18:29580657..29586167hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg385511
hg195511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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