A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419407



Internal ID21076960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115666901..115669800hg38UCSC Ensembl
chr8:116679128..116682027hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226920
Samples
Known GenesTRPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419407
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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