A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225865



Internal ID22368870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99588351..99591900hg38UCSC Ensembl
chr14:100054688..100058237hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383550
hg193550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14374671, nssv14374046, nssv14384918, nssv14391752, nssv14375897, nssv14390888, nssv14380433, nssv14375228, nssv14387892
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesCCDC85C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225865
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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