A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091191



Internal ID15944377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:94720527..94911104hg38UCSC Ensembl
Innerchr7:94349839..94540416hg19UCSC Ensembl
Innerchr7:94187775..94378352hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38190578
hg19190578
hg18190578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607858
Supporting Variants
Samples
Known GenesPPP1R9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091191
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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