A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193032



Internal ID20760073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95083876..95307720hg38UCSC Ensembl
chr13:95736130..95959974hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38223845
hg19223845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488260
Supporting Variants
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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