A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431203



Internal ID22489073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80269341..80276388hg38UCSC Ensembl
chr8:81181576..81188623hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg387048
hg197048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431203
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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