A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585761



Internal ID16373170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25911935..26319041hg38UCSC Ensembl
Innerchr20:25892571..26299677hg19UCSC Ensembl
Innerchr20:25840571..26247677hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38407107
hg19407107
hg18407107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938990
Samples
Known GenesFAM182A, LOC100134868, LOC284801, MIR663A, NCOR1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585761
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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