A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039050



Internal ID18781581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7162772..7190800hg38UCSC Ensembl
Innerchr16:7212773..7240801hg19UCSC Ensembl
Innerchr16:7152774..7180802hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3828029
hg1928029
hg1828029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2716n100
Supporting Variantsnssv3718866
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039050
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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