A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568814



Internal ID16356223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483399..31483974hg38UCSC Ensembl
Innerchr15:31775602..31776177hg19UCSC Ensembl
Innerchr15:29562894..29563469hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38576
hg19576
hg18576
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4436n54
Supporting Variantsnssv839608, nssv839614, nssv839612, nssv839613, nssv839607, nssv839615, nssv839609, nssv839610, nssv839611
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568814
Frequency
Sample Size17421
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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