A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053454



Internal ID19142673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87242912..87327490hg38UCSC Ensembl
Innerchr15:87786143..87870721hg19UCSC Ensembl
Innerchr15:85587147..85671725hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3884579
hg1984579
hg1884579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555100
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053454
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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