A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569779



Internal ID16357188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65525189..65530196hg38UCSC Ensembl
Innerchr15:65817527..65822534hg19UCSC Ensembl
Innerchr15:63604580..63609587hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385008
hg195008
hg185008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4577n54
Supporting Variantsnssv844269
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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