A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571396



Internal ID16012119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7370485..7392292hg38UCSC Ensembl
Innerchr16:7420486..7442293hg19UCSC Ensembl
Innerchr16:7360487..7382294hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3821808
hg1921808
hg1821808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150511
SamplesHGDP00839
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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