A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560087



Internal ID22428882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6227195..6227195hg38UCSC Ensembl
chr12:6336361..6336361hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362605, nssv14362604
SamplesNA19238, NA19240
Known GenesCD9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560087
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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