A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527401



Internal ID22396787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68949176..68949330hg38UCSC Ensembl
chr7:68414163..68414317hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336494, nssv14336500, nssv14336499, nssv14336495, nssv14336492, nssv14336497, nssv14336498, nssv14336496, nssv14336493
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527401
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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