A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037500



Internal ID18780031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6837688..6915297hg38UCSC Ensembl
Innerchr16:6887689..6965298hg19UCSC Ensembl
Innerchr16:6827690..6905299hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3877610
hg1977610
hg1877610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2711n100
Supporting Variantsnssv3718856
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)nsv1037500
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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