A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038232



Internal ID19127451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119888635..119914356hg38UCSC Ensembl
Innerchr11:119759344..119785065hg19UCSC Ensembl
Innerchr11:119264554..119290275hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3825722
hg1925722
hg1825722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508368
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)nsv1038232
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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