A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556578



Internal ID15997301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131680956..131688574hg38UCSC Ensembl
Innerchr11:131550850..131558468hg19UCSC Ensembl
Innerchr11:131056060..131063678hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg387619
hg197619
hg187619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2200n54
Supporting Variantsnssv785117, nssv785118
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556578
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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