A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571727



Internal ID16359136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28390583..28414773hg38UCSC Ensembl
Innerchr16:28401904..28426094hg19UCSC Ensembl
Innerchr16:28309405..28333595hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3824191
hg1924191
hg1824191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4966n54
Supporting Variantsnssv855255
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)nsv571727
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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