A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044847



Internal ID19134066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65168343..65302258hg38UCSC Ensembl
Innerchr13:65742475..65876390hg19UCSC Ensembl
Innerchr13:64640476..64774391hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38133916
hg19133916
hg18133916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3527914
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)nsv1044847
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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