A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417206



Internal ID21074759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58101601..58105700hg38UCSC Ensembl
chr8:59014160..59018259hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169949
Samples
Known GenesFAM110B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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