A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198009



Internal ID20765049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9993744..10135957hg38UCSC Ensembl
chr18:9993741..10135954hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38142214
hg19142214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198009
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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