A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111892



Internal ID21295158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30083966..30090610hg38UCSC Ensembl
Innerchr12:30236899..30243543hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg386645
hg196645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv241n145
Supporting Variantsnssv14093789, nssv14092733, nssv14090342, nssv14092799, nssv14092905
Samplessample156, sample7, sample130, sample364, sample113
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111892
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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