A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092079



Internal ID15945265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:107077902..107112803hg38UCSC Ensembl
Innerchr7:106718347..106753248hg19UCSC Ensembl
Innerchr7:106505583..106540484hg18UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3834902
hg1934902
hg1834902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608072
Supporting Variants
Samples
Known GenesPRKAR2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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