A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068650



Internal ID21503460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124306124..124306303hg38UCSC Ensembl
chr10:125994693..125994872hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602007
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068650
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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