A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202501



Internal ID22351657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2271569..2271688hg38UCSC Ensembl
chr5:2271683..2271802hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7150n152
Supporting Variantsnssv14320725, nssv14320726
SamplesNA19238, NA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202501
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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