A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044572



Internal ID19133791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13870592..13890828hg38UCSC Ensembl
Innerchr11:13892139..13912375hg19UCSC Ensembl
Innerchr11:13848715..13868951hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3820237
hg1920237
hg1820237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516261
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)nsv1044572
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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