A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526711



Internal ID22396094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27359344..27359460hg38UCSC Ensembl
chr2:27582211..27582327hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4530n152
Supporting Variantsnssv14292062, nssv14292063, nssv14292061, nssv14292060
SamplesNA19239, HG00731, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526711
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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