A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225217



Internal ID20792257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35507944..35546005hg38UCSC Ensembl
chr6:35475721..35513782hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3838062
hg1938062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401356
Supporting Variants
Samples
Known GenesTULP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225217
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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