A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037531



Internal ID19126750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127290188..127323671hg38UCSC Ensembl
Innerchr11:127160083..127193566hg19UCSC Ensembl
Innerchr11:126665293..126698776hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3833484
hg1933484
hg1833484
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505071
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)nsv1037531
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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