A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068890



Internal ID21451242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127915738..127915738hg38UCSC Ensembl
chr10:129714002..129714002hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642560
Supporting Variants
SamplesHG01505
Known GenesPTPRE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068890
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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