A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129809



Internal ID21460053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146279870..146279870hg38UCSC Ensembl
chr3:145997657..145997657hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616735
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129809
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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