A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196508



Internal ID20763548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93788157..93851872hg38UCSC Ensembl
chr10:95547914..95611629hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3863716
hg1963716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437521
Supporting Variants
Samples
Known GenesLGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196508
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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