A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569338



Internal ID16010061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48104611..48160602hg38UCSC Ensembl
Innerchr15:48396808..48452799hg19UCSC Ensembl
Innerchr15:46184100..46240091hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3855992
hg1955992
hg1855992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842497
Samples
Known GenesMYEF2, SLC24A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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