A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134866



Internal ID21411305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131357263..131357263hg38UCSC Ensembl
chr3:131076107..131076107hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616159
Supporting Variants
SamplesHG00513
Known GenesLOC339874
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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