A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036806



Internal ID19126025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97208359..98061073hg38UCSC Ensembl
Innerchr11:97079359..97931801hg19UCSC Ensembl
Innerchr11:96584569..97437011hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38852715
hg19852443
hg18852443
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505495
Samples
Known GenesMIR7976
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036806
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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