A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224059



Internal ID22367616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39466301..39469450hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv893n152
Supporting Variantsnssv14343125, nssv14343127, nssv14343129, nssv14343126, nssv14343130, nssv14343123, nssv14343128, nssv14343131, nssv14343124
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224059
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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