A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569323



Internal ID16356732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46904168..46988457hg38UCSC Ensembl
Innerchr15:47196366..47280655hg19UCSC Ensembl
Innerchr15:44983658..45067947hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3884290
hg1984290
hg1884290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149594
Samples1780862530_A
Known GenesMIR548A3, MIR548U
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569323
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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