A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559087



Internal ID22421666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86469247..86469247hg38UCSC Ensembl
chr10:88229004..88229004hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355494, nssv14355495, nssv14355496
SamplesNA19238, NA19239, NA19240
Known GenesWAPAL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559087
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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