A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219056



Internal ID20786096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99606413..99627797hg38UCSC Ensembl
chr6:100054289..100075673hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3821385
hg1921385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608127
Supporting Variants
Samples
Known GenesPRDM13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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