A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429068



Internal ID21086621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67331285..67334009hg38UCSC Ensembl
chr8:68243520..68246244hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170531
Samples
Known GenesARFGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429068
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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