A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423458



Internal ID21081011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81460174..81461158hg38UCSC Ensembl
chr8:82372409..82373393hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171914
Samples
Known GenesFABP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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