A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529596



Internal ID22398988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123935960..123936097hg38UCSC Ensembl
chr10:125695476..125695613hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355213, nssv14355212, nssv14355214
SamplesHG00512, HG00732, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529596
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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