A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571332



Internal ID16012055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6583079..6626446hg38UCSC Ensembl
Innerchr16:6633080..6676447hg19UCSC Ensembl
Innerchr16:6573081..6616448hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3843368
hg1943368
hg1843368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4889n54
Supporting Variantsnssv1148916
SamplesHGDP00978
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571332
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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