A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433181



Internal ID21090734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66961201..66963400hg38UCSC Ensembl
chr8:67873436..67875635hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225709
Samples
Known GenesTCF24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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