A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037145



Internal ID19126364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15796962..15809392hg38UCSC Ensembl
Innerchr11:15818508..15830938hg19UCSC Ensembl
Innerchr11:15775084..15787514hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3812431
hg1912431
hg1812431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504747
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)nsv1037145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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