A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571166



Internal ID16011889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1582964..1694025hg38UCSC Ensembl
Innerchr16:1632965..1744026hg19UCSC Ensembl
Innerchr16:1572966..1684027hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38111062
hg19111062
hg18111062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4855n54
Supporting Variantsnssv852058
Samples
Known GenesCRAMP1L, HN1L, IFT140
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571166
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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