A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561389



Internal ID16348798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28417851..28477194hg38UCSC Ensembl
Innerchr13:28991988..29051331hg19UCSC Ensembl
Innerchr13:27889988..27949331hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3859344
hg1959344
hg1859344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176346
Samples1780854101_A
Known GenesFLT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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