A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197147



Internal ID20764187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71271773..71324777hg38UCSC Ensembl
chr18:68939009..68992013hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3853005
hg1953005
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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