A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570358



Internal ID16357767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86596552..86666536hg38UCSC Ensembl
Innerchr15:87139783..87209767hg19UCSC Ensembl
Innerchr15:84940787..85010771hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3869985
hg1969985
hg1869985
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848133
Samples
Known GenesAGBL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570358
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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