A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052612



Internal ID18795143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6844259..7020642hg38UCSC Ensembl
Innerchr16:6894260..7070643hg19UCSC Ensembl
Innerchr16:6834261..7010644hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38176384
hg19176384
hg18176384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2712n100
Supporting Variantsnssv3557063
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)nsv1052612
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