A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638672



Internal ID21586977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70831965..70831965hg38UCSC Ensembl
chr9:73446881..73446881hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162793
SamplesHG03125
Known GenesTRPM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638672
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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