A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117867



Internal ID21301133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178982843..179005655hg38UCSC Ensembl
Innerchr1:178951978..178974790hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3822813
hg1922813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv89n145
Supporting Variantsnssv14086731, nssv14085069, nssv14089141, nssv14101457
Samplessample206, sample169, sample397, sample194
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117867
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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