A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569805



Internal ID16357214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68087284..68112024hg38UCSC Ensembl
Innerchr15:68379622..68404362hg19UCSC Ensembl
Innerchr15:66166676..66191416hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3824741
hg1924741
hg1824741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844365
Samples
Known GenesPIAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569805
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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