A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235982



Internal ID20803022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63562391..63575785hg38UCSC Ensembl
chr6:64272296..64285690hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3813395
hg1913395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408475
Supporting Variants
Samples
Known GenesPTP4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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