A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047833



Internal ID18790364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76160196..76198575hg38UCSC Ensembl
Innerchr11:75871240..75909619hg19UCSC Ensembl
Innerchr11:75548888..75587267hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3838380
hg1938380
hg1838380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1226n100
Supporting Variantsnssv3517390, nssv3509784
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)nsv1047833
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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