A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195756



Internal ID20762796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110632625..111083620hg38UCSC Ensembl
chr13:111284972..111735967hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38450996
hg19450996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483799
Supporting Variants
Samples
Known GenesANKRD10, CARKD, CARS2, ING1, LINC00346
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195756
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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