A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037940



Internal ID18780471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76144272..76198575hg38UCSC Ensembl
Innerchr11:75855316..75909619hg19UCSC Ensembl
Innerchr11:75532964..75587267hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3854304
hg1954304
hg1854304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504444
Samples
Known GenesWNT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037940
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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