A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529997



Internal ID22399388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67414288..67414778hg38UCSC Ensembl
chr11:67181759..67182249hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360537, nssv14360539, nssv14360538, nssv14360540
SamplesHG00512, NA19239, HG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529997
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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