A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529739



Internal ID22399130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59672310..59672372hg38UCSC Ensembl
chr11:59439783..59439845hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1401n152
Supporting Variantsnssv14358975, nssv14358974
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529739
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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