A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068773



Internal ID21401150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13128573..13129383hg38UCSC Ensembl
chr10:13170573..13171383hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598404
Supporting Variants
SamplesHG00096
Known GenesOPTN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068773
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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