A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568815



Internal ID16356224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483399..31484086hg38UCSC Ensembl
Innerchr15:31775602..31776289hg19UCSC Ensembl
Innerchr15:29562894..29563581hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38688
hg19688
hg18688
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4436n54
Supporting Variantsnssv839618, nssv839617, nssv839620, nssv839626, nssv839623, nssv839628, nssv839622, nssv839627, nssv839625, nssv839624, nssv839621, nssv839619, nssv839616
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568815
Frequency
Sample Size17421
Observed Gain9
Observed Loss4
Observed Complex0
Frequencyn/a


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