A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045641



Internal ID19134860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27665667..27682648hg38UCSC Ensembl
Innerchr15:27910813..27927794hg19UCSC Ensembl
Innerchr15:25584408..25601389hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3816982
hg1916982
hg1816982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2487n100
Supporting Variantsnssv3545641, nssv3545640, nssv3545643, nssv3545644, nssv3545639, nssv3545638, nssv3545642
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)nsv1045641
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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