A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180199



Internal ID20747239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77474209..77507493hg38UCSC Ensembl
chr13:78048344..78081628hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3833285
hg1933285
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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