A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430570



Internal ID21088123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124034622..124041709hg38UCSC Ensembl
chr8:125046863..125053950hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg387088
hg197088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164042
Samples
Known GenesFER1L6, FER1L6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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