A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3520355



Internal ID22389763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29132867..29132935hg38UCSC Ensembl
chr10:29421796..29421864hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338300, nssv14338305, nssv14338301, nssv14338306, nssv14338302, nssv14338303, nssv14338304, nssv14338299
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3520355
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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