A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17007917



Internal ID72902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:754288..754778hg38UCSC Ensembl
chr8:704288..704778hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481306
Supporting Variants
Samples
Known GenesERICH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17007917
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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