A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611357



Internal ID16398766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:52532940..52593195hg38UCSC Ensembl
Innerchr8:53445500..53505755hg19UCSC Ensembl
Innerchr8:53608053..53668308hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3860256
hg1960256
hg1860256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115325
Samples
Known GenesFAM150A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611357
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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