A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435314



Internal ID21092867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92713815..92714641hg38UCSC Ensembl
chr8:93726043..93726869hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173476
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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