A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571629



Internal ID16012352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21569823..21747375hg38UCSC Ensembl
Innerchr16:21581144..21758696hg19UCSC Ensembl
Innerchr16:21488645..21666197hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38177553
hg19177553
hg18177553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4944n54
Supporting Variantsnssv853101
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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