A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798869



Internal ID16092825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:77422387..77513838hg38UCSC Ensembl
Innerchr12:77816167..77907618hg19UCSC Ensembl
Innerchr12:76340298..76431749hg18UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3891452
hg1991452
hg1891452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559427
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)nssv798869
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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