A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528764



Internal ID22398155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49335417..49335653hg38UCSC Ensembl
chr10:50543462..50543698hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv926n152
Supporting Variantsnssv14343832, nssv14343835, nssv14343834, nssv14343831, nssv14343833
SamplesHG00512, NA19238, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528764
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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