A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995193



Internal ID16289149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28736466..28871211hg38UCSC Ensembl
Innerchr4:28738088..28872833hg19UCSC Ensembl
Innerchr4:28347186..28481931hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38134746
hg19134746
hg18134746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593894
Supporting Variants
Samples
Known GenesMIR4275
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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