A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588891



Internal ID21780934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96376368..96376565hg38UCSC Ensembl
chr8:97388596..97388793hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588891
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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