A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571735



Internal ID16359144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28406425..28414518hg38UCSC Ensembl
Innerchr16:28417746..28425839hg19UCSC Ensembl
Innerchr16:28325247..28333340hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg388094
hg198094
hg188094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4968n54
Supporting Variantsnssv855265, nssv855264
Samples
Known GenesEIF3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571735
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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