A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048469



Internal ID19137688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66576621..66598750hg38UCSC Ensembl
Innerchr15:66868959..66891088hg19UCSC Ensembl
Innerchr15:64656013..64678142hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3822130
hg1922130
hg1822130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717956
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)nsv1048469
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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