A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585411



Internal ID16372820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9616908..10002652hg38UCSC Ensembl
Innerchr20:9597555..9983300hg19UCSC Ensembl
Innerchr20:9545555..9931300hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38385745
hg19385746
hg18385746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv937957
Samples
Known GenesPAK7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585411
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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