A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571395



Internal ID16012118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7355610..7429131hg38UCSC Ensembl
Innerchr16:7405611..7479132hg19UCSC Ensembl
Innerchr16:7345612..7419133hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3873522
hg1973522
hg1873522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150510
Samples1780846005_A
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571395
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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