A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041112



Internal ID18783643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113198424..113243503hg38UCSC Ensembl
Innerchr9:115960704..116005783hg19UCSC Ensembl
Innerchr9:115000525..115045604hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3845080
hg1945080
hg1845080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695151
Samples
Known GenesFKBP15, SLC31A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041112
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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