A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048366



Internal ID19137585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87014673..87043476hg38UCSC Ensembl
Innerchr15:87557904..87586707hg19UCSC Ensembl
Innerchr15:85358908..85387711hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3828804
hg1928804
hg1828804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555098
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)nsv1048366
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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