A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528145



Internal ID22397529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120798394..120798510hg38UCSC Ensembl
chr10:122557906..122558022hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1079n152
Supporting Variantsnssv14355103, nssv14355104, nssv14355105
SamplesNA19239, HG00732, NA19240
Known GenesMIR5694, WDR11-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528145
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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