A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420488



Internal ID21078041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6688593..6810632hg38UCSC Ensembl
chr8:6546114..6668153hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38122040
hg19122040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169429
Samples
Known GenesAGPAT5, MIR4659A, MIR4659B, XKR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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