A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192258



Internal ID20759298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111938190..112596067hg38UCSC Ensembl
chr10:113697948..114355826hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38657878
hg19657879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446012
Supporting Variants
Samples
Known GenesACSL5, GPAM, GUCY2GP, MIR6715A, MIR6715B, TECTB, VTI1A, ZDHHC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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