A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431507



Internal ID21089060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139095871..139096909hg38UCSC Ensembl
chr8:140108114..140109152hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431507
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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