A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569793



Internal ID16010516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66047062..66308291hg38UCSC Ensembl
Innerchr15:66339400..66600629hg19UCSC Ensembl
Innerchr15:64126454..64387683hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38261230
hg19261230
hg18261230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844317
Samples
Known GenesDIS3L, MEGF11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569793
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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