A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610014



Internal ID16050737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6934193..6936878hg38UCSC Ensembl
Innerchr8:6791715..6794400hg19UCSC Ensembl
Innerchr8:6779125..6781810hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382686
hg192686
hg182686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11906n54
Supporting Variantsnssv1105685
Samples
Known GenesDEFA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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