A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174298



Internal ID15529666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49089915..49935211hg38UCSC Ensembl
Innerchr11:49111467..49956763hg19UCSC Ensembl
Innerchr11:49068043..49913339hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38845297
hg19845297
hg18845297
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554347
Supporting Variants
SamplesHGDP00825
Known GenesFOLH1, LOC440040
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174298
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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