A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557689



Internal ID16345098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:19316144..19431199hg38UCSC Ensembl
Innerchr12:19469078..19584133hg19UCSC Ensembl
Innerchr12:19360345..19475400hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38115056
hg19115056
hg18115056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2397n54
Supporting Variantsnssv789499, nssv789500
Samples
Known GenesPLEKHA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557689
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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