A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv786743



Internal ID16080699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:3999347..4055649hg38UCSC Ensembl
Innerchr12:4108513..4164815hg19UCSC Ensembl
Innerchr12:3978774..4035076hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3856303
hg1956303
hg1856303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557120
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv786743
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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