A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559772



Internal ID21884127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:751080..751157hg38UCSC Ensembl
chr8:701080..701157hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019623
Supporting Variants
Samples
Known GenesERICH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559772
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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