A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612534



Internal ID16399943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:138747361..139100651hg38UCSC Ensembl
Innerchr8:139759604..140112894hg19UCSC Ensembl
Innerchr8:139828786..140182076hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38353291
hg19353291
hg18353291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1124230
Samples
Known GenesCOL22A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612534
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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