A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008986



Internal ID22070617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27942560..27944711hg38UCSC Ensembl
Outerchr12:27941988..27950527hg38UCSC Ensembl
Innerchr12:28095493..28097644hg19UCSC Ensembl
Outerchr12:28094921..28103460hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg388540
hg198540
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154819
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008986
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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