A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071769



Internal ID21452472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89142617..89142667hg38UCSC Ensembl
chr10:90902374..90902424hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591559
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071769
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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