A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419924



Internal ID21077477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130892361..130892764hg38UCSC Ensembl
chr8:131904607..131905010hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165108
Samples
Known GenesADCY8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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