A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528495



Internal ID22397883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74050702..74051277hg38UCSC Ensembl
chr11:73761747..73762322hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357873, nssv14357872
SamplesNA19239, NA19240
Known GenesC2CD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528495
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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