A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197585



Internal ID20764625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67193601..67274300hg38UCSC Ensembl
chr18:64860838..64941537hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3880700
hg1980700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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