A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054189



Internal ID19143408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27665667..27683648hg38UCSC Ensembl
Innerchr15:27910813..27928794hg19UCSC Ensembl
Innerchr15:25584408..25602389hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3817982
hg1917982
hg1817982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2487n100
Supporting Variantsnssv3545645
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)nsv1054189
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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