A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430919



Internal ID21088472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138398345..138401791hg38UCSC Ensembl
chr8:139410588..139414034hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg383447
hg193447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166438
Samples
Known GenesFAM135B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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