A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030711



Internal ID88181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10292266..10294427hg38UCSC Ensembl
chr10:10334229..10336390hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382162
hg192162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480989
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030711
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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