A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063489



Internal ID18806020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29978176..30028098hg38UCSC Ensembl
Innerchr19:30469083..30519005hg19UCSC Ensembl
Innerchr19:35160923..35210845hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3849923
hg1949923
hg1849923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3513n100
Supporting Variantsnssv3566564
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063489
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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