A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035605



Internal ID19124824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27771985..27794973hg38UCSC Ensembl
Innerchr11:27793532..27816520hg19UCSC Ensembl
Innerchr11:27750108..27773096hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3822989
hg1922989
hg1822989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710072
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)nsv1035605
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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