A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434124



Internal ID21091677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124482901..124492700hg38UCSC Ensembl
chr8:125495142..125504941hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164071
Samples
Known GenesRNF139, TATDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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