A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214564



Internal ID20781605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12012901..12023500hg38UCSC Ensembl
chr6:12013134..12023733hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406064
Supporting Variants
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00084


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