A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035467



Internal ID91387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64924625..64928155hg38UCSC Ensembl
chr10:66684383..66687913hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383531
hg193531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035467
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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