A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606399



Internal ID21554704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113935074..113935074hg38UCSC Ensembl
chr3:113653921..113653921hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123872
SamplesNA12329
Known GenesGRAMD1C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606399
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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