A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171118



Internal ID20738158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:787607..863146hg38UCSC Ensembl
chr8:737607..813146hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3875540
hg1975540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422726
Supporting Variants
Samples
Known GenesERICH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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