A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420112



Internal ID21077665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123813001..123814300hg38UCSC Ensembl
chr8:124825241..124826540hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164024
Samples
Known GenesFAM91A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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