A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170749



Internal ID20737789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88674179..88702835hg38UCSC Ensembl
chr8:89686408..89715064hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3828657
hg1928657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00183


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