A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616142



Internal ID18914423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3899113..4165406hg38UCSC Ensembl
Innerchr4:3900840..4167133hg19UCSC Ensembl
Innerchr4:3870638..4218034hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38266294
hg19266294
hg18347397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008883
Supporting Variants
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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