A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14307731



Internal ID22118999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107406264..107406489hg38UCSC Ensembl
chr3:107125111..107125336hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525144
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14307731
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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