A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199169



Internal ID22348794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194152411..194152468hg38UCSC Ensembl
chr3:193870200..193870257hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6317n152
Supporting Variantsnssv14310274, nssv14310275, nssv14310276
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199169
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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