A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053580



Internal ID18796111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76160196..76193582hg38UCSC Ensembl
Innerchr11:75871240..75904626hg19UCSC Ensembl
Innerchr11:75548888..75582274hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3833387
hg1933387
hg1833387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1226n100
Supporting Variantsnssv3513809, nssv3522335, nssv3507189, nssv3511982, nssv3513632, nssv3504578, nssv3517931
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)nsv1053580
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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