A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14310141



Internal ID22139603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181897360..181897998hg38UCSC Ensembl
chr3:181615148..181615786hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195844
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14310141
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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