A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571179



Internal ID16011902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1947613..1995730hg38UCSC Ensembl
Innerchr16:1997614..2045731hg19UCSC Ensembl
Innerchr16:1937615..1985732hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3848118
hg1948118
hg1848118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852074
Samples
Known GenesGFER, NDUFB10, NOXO1, RNF151, RPL3L, RPS2, SNHG9, SNORA10, SNORA64, SNORA78, SYNGR3, TBL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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