A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048589



Internal ID18791120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67736173..67981775hg38UCSC Ensembl
Innerchr11:67503644..67749246hg19UCSC Ensembl
Innerchr11:67260220..67505822hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38245603
hg19245603
hg18245603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1215n100
Supporting Variantsnssv3710633
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048589
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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