A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170434



Internal ID20737474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77597859..77607978hg38UCSC Ensembl
chr8:78510095..78520214hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3810120
hg1910120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431023
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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