A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135731



Internal ID21406417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140883228..140883228hg38UCSC Ensembl
chr3:140602070..140602070hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624122
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135731
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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