A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527751



Internal ID22397138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33907183..33907278hg38UCSC Ensembl
chr10:34196111..34196206hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv867n152
Supporting Variantsnssv14339265, nssv14339267, nssv14339266
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527751
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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