A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558621



Internal ID21882976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27670688..27670741hg38UCSC Ensembl
chr8:27528205..27528258hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001325
Supporting Variants
Samples
Known GenesSCARA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558621
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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