A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852257



Internal ID15799527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2904265..2942113hg38UCSC Ensembl
Innerchr16:2954266..2992114hg19UCSC Ensembl
Innerchr16:2894267..2932115hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3837849
hg1937849
hg1837849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571245
Supporting Variants
Samples
Known GenesFLYWCH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852257
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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