A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052829



Internal ID18795360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107816082..107854571hg38UCSC Ensembl
Innerchr11:107686808..107725297hg19UCSC Ensembl
Innerchr11:107192018..107230507hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3838490
hg1938490
hg1838490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1277n100
Supporting Variantsnssv3519541, nssv3710746
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052829
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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