A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947334



Internal ID21367403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9086726..9086726hg38UCSC Ensembl
chr3:9128410..9128410hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187516
SamplesHG002
Known GenesSRGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947334
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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