A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125617



Internal ID21488041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105902474..105902474hg38UCSC Ensembl
chr3:105621321..105621321hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612082
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125617
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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