A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570186



Internal ID16357595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77818989..77820182hg38UCSC Ensembl
Innerchr15:78111331..78112524hg19UCSC Ensembl
Innerchr15:75898386..75899579hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg381194
hg191194
hg181194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4669n54
Supporting Variantsnssv847407, nssv847406, nssv847410, nssv847408, nssv847405, nssv847404, nssv847409
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570186
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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