A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv792363



Internal ID16086319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33149504..33181327hg38UCSC Ensembl
Innerchr12:33302438..33334261hg19UCSC Ensembl
Innerchr12:33193705..33225528hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3831824
hg1931824
hg1831824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558218
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)nssv792363
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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