A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179683



Internal ID20746723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97972101..97984400hg38UCSC Ensembl
chr13:98624355..98636654hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3812300
hg1912300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482718
Supporting Variants
Samples
Known GenesIPO5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179683
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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