A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044773



Internal ID18787304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67766314..67969010hg38UCSC Ensembl
Innerchr11:67533785..67736481hg19UCSC Ensembl
Innerchr11:67290361..67493057hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38202697
hg19202697
hg18202697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1219n100
Supporting Variantsnssv3511277
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)nsv1044773
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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