A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526059



Internal ID22395439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17216972..17217031hg38UCSC Ensembl
chr2:17398239..17398298hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14288321, nssv14288322
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526059
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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