A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571386



Internal ID16012109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6987386..7015507hg38UCSC Ensembl
Innerchr16:7037387..7065508hg19UCSC Ensembl
Innerchr16:6977388..7005509hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3828122
hg1928122
hg1828122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4899n54
Supporting Variantsnssv852414
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571386
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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