A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221855



Internal ID20788895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84932542..85530787hg38UCSC Ensembl
chr6:85642260..86240505hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38598246
hg19598246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412928
Supporting Variants
Samples
Known GenesNT5E, SNX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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