A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131177



Internal ID21406079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126260396..126260396hg38UCSC Ensembl
chr3:125979239..125979239hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611897
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131177
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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