A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182128



Internal ID20749168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41327735..41339438hg38UCSC Ensembl
chr13:41901871..41913574hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3811704
hg1911704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476657
Supporting Variants
Samples
Known GenesNAA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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