A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009242



Internal ID22070873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:68362591..68371456hg38UCSC Ensembl
Outerchr12:68361763..68374559hg38UCSC Ensembl
Innerchr12:68756371..68765236hg19UCSC Ensembl
Outerchr12:68755543..68768339hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3812797
hg1912797
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154839
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009242
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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