A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039254



Internal ID18781785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86527126..87399757hg38UCSC Ensembl
Innerchr15:87070357..87942988hg19UCSC Ensembl
Innerchr15:84871361..85743992hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38872632
hg19872632
hg18872632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555095
Samples
Known GenesAGBL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039254
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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