A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194477



Internal ID20761517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31013227..31024620hg38UCSC Ensembl
chr10:31302156..31313549hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811394
hg1911394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449040
Supporting Variants
Samples
Known GenesZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00122


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