A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068402



Internal ID21483452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119559467..119559585hg38UCSC Ensembl
chr10:121318979..121319097hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604278
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068402
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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