A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585871



Internal ID16373280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30377730..30413519hg38UCSC Ensembl
Innerchr20:29612406..29648195hg19UCSC Ensembl
Innerchr20:28226067..28261856hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3835790
hg1935790
hg1835790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7548n54
Supporting Variantsnssv939194
Samples
Known GenesFRG1B, MLLT10P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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