A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228151



Internal ID22370425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7838906..7844549hg38UCSC Ensembl
chr10:7880869..7886512hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385644
hg195644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14328863, nssv14328870, nssv14328871, nssv14328868, nssv14328864, nssv14328867, nssv14328866, nssv14328865, nssv14328869
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesTAF3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228151
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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