A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111701



Internal ID21294967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119880476..119901890hg38UCSC Ensembl
Innerchr1:120423099..120444513hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3821415
hg1921415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv68n145
Supporting Variantsnssv14085670
Samplessample211
Known GenesADAM30
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111701
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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