A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045854



Internal ID18788385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76160196..76197866hg38UCSC Ensembl
Innerchr11:75871240..75908910hg19UCSC Ensembl
Innerchr11:75548888..75586558hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3837671
hg1937671
hg1837671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1226n100
Supporting Variantsnssv3511678, nssv3511006
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)nsv1045854
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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