A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187516



Internal ID21326349
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947334
Supporting Variants
SamplesHG002
Known GenesSRGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187516
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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