A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228492



Internal ID22370660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114138084..114138310hg38UCSC Ensembl
chr10:115897843..115898069hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354600, nssv14354598, nssv14354599
SamplesHG00731, HG00732, HG00513
Known GenesC10orf118
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228492
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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