A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045325



Internal ID18787856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6647561..6724695hg38UCSC Ensembl
Innerchr16:6697562..6774696hg19UCSC Ensembl
Innerchr16:6637563..6714697hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3877135
hg1977135
hg1877135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557045
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)nsv1045325
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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