A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556430



Internal ID15997153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:108226606..108304735hg38UCSC Ensembl
Innerchr11:108097333..108175462hg19UCSC Ensembl
Innerchr11:107602543..107680672hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3878130
hg1978130
hg1878130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784563
Samples
Known GenesATM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556430
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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