A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118069



Internal ID21301335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:85575385..85581734hg38UCSC Ensembl
Innerchr1:86041068..86047417hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg386350
hg196350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096652
Samplessample136
Known GenesCYR61, DDAH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118069
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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