A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009354



Internal ID18751885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:88804763..89064004hg38UCSC Ensembl
Innerchr4:89725914..89985155hg19UCSC Ensembl
Innerchr4:89944937..90204178hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38259242
hg19259242
hg18259242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633932
Samples
Known GenesFAM13A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009354
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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