A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640788



Internal ID21589093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137721130..137721130hg38UCSC Ensembl
chr9:140615582..140615582hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161298
SamplesNA19239
Known GenesEHMT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640788
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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