A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196853



Internal ID20763893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85964601..85967900hg38UCSC Ensembl
chr13:86538736..86542035hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196853
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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