A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712942



Internal ID16006898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47416966..47417275hg38UCSC Ensembl
Innerchr1:47882638..47882947hg19UCSC Ensembl
Innerchr1:47655225..47655534hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38310
hg19310
hg18310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546180
Supporting Variants
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712942
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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