A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588657



Internal ID21780700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88480979..88481085hg38UCSC Ensembl
chr8:89493208..89493314hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588657
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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