A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556568



Internal ID15997291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130070036..130070946hg38UCSC Ensembl
Innerchr11:129939931..129940841hg19UCSC Ensembl
Innerchr11:129445141..129446051hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2199n54
Supporting Variantsnssv785103
Samples
Known GenesAPLP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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