A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14307865



Internal ID22312579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86767545..86767606hg38UCSC Ensembl
chr3:86816695..86816756hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526653
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14307865
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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