A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv788949



Internal ID16082905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:15865952..15881634hg38UCSC Ensembl
Innerchr12:16018886..16034568hg19UCSC Ensembl
Innerchr12:15910153..15925835hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3815683
hg1915683
hg1815683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557625
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)nssv788949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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