A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033783



Internal ID90219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23800667..23801705hg38UCSC Ensembl
chr10:24089596..24090634hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg381039
hg191039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485749
Supporting Variants
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033783
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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