A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043115



Internal ID18785646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6658811..6818872hg38UCSC Ensembl
Innerchr16:6708812..6868873hg19UCSC Ensembl
Innerchr16:6648813..6808874hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38160062
hg19160062
hg18160062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557046
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)nsv1043115
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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