A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556569



Internal ID15997292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130070036..130071002hg38UCSC Ensembl
Innerchr11:129939931..129940897hg19UCSC Ensembl
Innerchr11:129445141..129446107hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38967
hg19967
hg18967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2198n54
Supporting Variantsnssv785105, nssv785104
Samples
Known GenesAPLP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556569
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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