A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17138657



Internal ID21452036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108030760..108030760hg38UCSC Ensembl
chr3:107749607..107749607hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382940
hg192940
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613090
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17138657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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