A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053179



Internal ID18795710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6606773..6643079hg38UCSC Ensembl
Innerchr16:6656774..6693080hg19UCSC Ensembl
Innerchr16:6596775..6633081hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3836307
hg1936307
hg1836307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2704n100
Supporting Variantsnssv3557033
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)nsv1053179
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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