A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604539



Internal ID21553209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9086726..9086726hg38UCSC Ensembl
chr3:9128410..9128410hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124433
SamplesHG00732
Known GenesSRGAP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604539
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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