A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010300



Internal ID22071931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:114970843..114977974hg38UCSC Ensembl
Outerchr12:114967297..114980205hg38UCSC Ensembl
Innerchr12:115408648..115415779hg19UCSC Ensembl
Outerchr12:115405102..115418010hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3812909
hg1912909
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154858
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010300
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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