A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568809



Internal ID16356218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483297..31484086hg38UCSC Ensembl
Innerchr15:31775500..31776289hg19UCSC Ensembl
Innerchr15:29562792..29563581hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38790
hg19790
hg18790
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4436n54
Supporting Variantsnssv839598, nssv839596, nssv839597, nssv839595, nssv839600, nssv839592, nssv839599, nssv839593, nssv839594
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568809
Frequency
Sample Size17421
Observed Gain6
Observed Loss3
Observed Complex0
Frequencyn/a


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