A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134425



Internal ID21473861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197022963..197022963hg38UCSC Ensembl
chr3:196749834..196749834hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604802
Supporting Variants
SamplesHG03371
Known GenesMFI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134425
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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