A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051654



Internal ID18794185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113119308..113173383hg38UCSC Ensembl
Innerchr9:115881588..115935663hg19UCSC Ensembl
Innerchr9:114921409..114975484hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3854076
hg1954076
hg1854076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695150
Samples
Known GenesFAM225A, FKBP15, SLC31A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051654
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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