A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528275



Internal ID22397661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122633342..122633407hg38UCSC Ensembl
chr10:124392858..124392923hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355172, nssv14355170, nssv14355171, nssv14355173
SamplesNA19238, HG00732, HG00513, HG00514
Known GenesDMBT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528275
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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