A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581706



Internal ID21773749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93645524..93647181hg38UCSC Ensembl
chr8:94657752..94659409hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013943
Supporting Variants
Samples
Known GenesLINC00535
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581706
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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