A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068147



Internal ID21435426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23790453..23790564hg38UCSC Ensembl
chr10:24079382..24079493hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594567
Supporting Variants
SamplesHG00731
Known GenesKIAA1217
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068147
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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