A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525076



Internal ID22394452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172570746..172570822hg38UCSC Ensembl
chr5:171997749..171997825hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7615n152
Supporting Variantsnssv14324505, nssv14324506
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525076
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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