A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173477



Internal ID20740517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92720001..92721200hg38UCSC Ensembl
chr8:93732229..93733428hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435581
Supporting Variants
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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