A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529089



Internal ID22398482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124239100..124239207hg38UCSC Ensembl
chr10:125927669..125927776hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355251, nssv14355248, nssv14355247, nssv14355249, nssv14355250
SamplesHG00512, NA19238, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529089
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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