A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571389



Internal ID16012112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7000339..7032044hg38UCSC Ensembl
Innerchr16:7050340..7082045hg19UCSC Ensembl
Innerchr16:6990341..7022046hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3831706
hg1931706
hg1831706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150507
SamplesHGDP00264
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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