A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633932



Internal ID18585527
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 StatusS
Merged Variantsnsv1009354
Supporting Variants
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)nssv3633932
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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