A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430707



Internal ID21088260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139600401..140174600hg38UCSC Ensembl
chr8:140612644..141184699hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38574200
hg19572056
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7524n223
Supporting Variantsnssv18221847
Samples
Known GenesKCNK9, TRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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