A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035532



Internal ID91433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65536368..65567200hg38UCSC Ensembl
chr10:67296126..67326958hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3830833
hg1930833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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