A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170435



Internal ID20737475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77602234..77645674hg38UCSC Ensembl
chr8:78514470..78557910hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3843441
hg1943441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431505
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170435
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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