A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553442



Internal ID16340851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7870146..7892364hg38UCSC Ensembl
Innerchr11:7891693..7913911hg19UCSC Ensembl
Innerchr11:7848269..7870487hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3822219
hg1922219
hg1822219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767045
Samples
Known GenesLOC283299
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553442
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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