A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569003



Internal ID21761046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27918643..27918697hg38UCSC Ensembl
chr8:27776160..27776214hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002672
Supporting Variants
Samples
Known GenesSCARA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569003
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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