A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053371



Internal ID18795902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6794991..6939148hg38UCSC Ensembl
Innerchr16:6844992..6989149hg19UCSC Ensembl
Innerchr16:6784993..6929150hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38144158
hg19144158
hg18144158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2708n100
Supporting Variantsnssv3718854
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)nsv1053371
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer