A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525944



Internal ID22395323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2025444..2025496hg38UCSC Ensembl
chr5:2025558..2025610hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320706, nssv14320709, nssv14320708, nssv14320707
SamplesNA19238, NA19239, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525944
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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