A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194519



Internal ID22344825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87802153..87802283hg38UCSC Ensembl
chr3:87851303..87851433hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6061n152
Supporting Variantsnssv14308083, nssv14308084
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194519
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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