A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642560



Internal ID21590865
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 StatusM
Merged Variants
Supporting Variantsnssv17068890
SamplesHG01505
Known GenesPTPRE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642560
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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