A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173476



Internal ID20740516
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 StatusS
Merged Variantsnsv6435314
Supporting Variants
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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