A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224648



Internal ID22368014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110208451..110209550hg38UCSC Ensembl
chr10:111968209..111969308hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353822, nssv14353816, nssv14353821, nssv14353815, nssv14353819, nssv14353817, nssv14353818, nssv14353820, nssv14353814
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesMXI1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224648
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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