A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17007372



Internal ID72553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10298000..10303163hg38UCSC Ensembl
chr8:10155510..10160673hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385164
hg195164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487144
Supporting Variants
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17007372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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