A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526599



Internal ID22395980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201683071..201683149hg38UCSC Ensembl
chr2:202547794..202547872hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14296283, nssv14296282
SamplesNA19238, NA19240
Known GenesMPP4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526599
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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