A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526290



Internal ID22395670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115654880..115654953hg38UCSC Ensembl
chr5:114990577..114990650hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7491n152
Supporting Variantsnssv14321767, nssv14321768, nssv14321765, nssv14321764, nssv14321770, nssv14321766, nssv14321771, nssv14321769
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesLOC102467217
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526290
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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