A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028991



Internal ID19118210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131546907..131626271hg38UCSC Ensembl
Innerchr4:132468062..132547426hg19UCSC Ensembl
Innerchr4:132687512..132766876hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3879365
hg1979365
hg1879365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639484
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028991
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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