A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117184



Internal ID21300450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:60949356..60956903hg38UCSC Ensembl
Innerchr1:61415028..61422575hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089593
Samplessample241
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117184
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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