A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219087



Internal ID22364219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13713817..13713876hg38UCSC Ensembl
chr10:13755817..13755876hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv813n152
Supporting Variantsnssv14332539, nssv14332540, nssv14332537, nssv14332535, nssv14332536, nssv14332533, nssv14332538, nssv14332534
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00514
Known GenesFRMD4A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219087
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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