A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049878



Internal ID19139097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32179274..32329014hg38UCSC Ensembl
Innerchr15:32471475..32621215hg19UCSC Ensembl
Innerchr15:30258767..30408507hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38149741
hg19149741
hg18149741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2540n100
Supporting Variantsnssv3721632
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)nsv1049878
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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