A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571726



Internal ID16359135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28390583..28407135hg38UCSC Ensembl
Innerchr16:28401904..28418456hg19UCSC Ensembl
Innerchr16:28309405..28325957hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3816553
hg1916553
hg1816553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4965n54
Supporting Variantsnssv855254
Samples
Known GenesEIF3C, EIF3CL, MIR6862-1, MIR6862-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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