A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571352



Internal ID16012075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6700249..7091209hg38UCSC Ensembl
Innerchr16:6750250..7141210hg19UCSC Ensembl
Innerchr16:6690251..7081211hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38390961
hg19390961
hg18390961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4892n54
Supporting Variantsnssv852382
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571352
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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