A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011831



Internal ID18754366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197671333..197845491hg38UCSC Ensembl
Innerchr3:197398204..197572362hg19UCSC Ensembl
Innerchr3:198882601..199056759hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38174159
hg19174159
hg18174159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3617025
Samples
Known GenesFYTTD1, KIAA0226, LRCH3, MIR922
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011831
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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