A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939193



Internal ID16233149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30369097..30413519hg38UCSC Ensembl
Innerchr20:29603773..29648195hg19UCSC Ensembl
Innerchr20:28217434..28261856hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3844423
hg1944423
hg1844423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585870
Supporting Variants
Samples
Known GenesFRG1B, MLLT10P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939193
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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