A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044894



Internal ID18787425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76160196..76253330hg38UCSC Ensembl
Innerchr11:75871240..75964374hg19UCSC Ensembl
Innerchr11:75548888..75642022hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3893135
hg1993135
hg1893135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1227n100
Supporting Variantsnssv3511399
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)nsv1044894
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer