A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032161



Internal ID18774695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161321132..162613846hg38UCSC Ensembl
Innerchr4:162242284..163534998hg19UCSC Ensembl
Innerchr4:162461734..163754448hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg381292715
hg191292715
hg181292715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5454n100
Supporting Variantsnssv3744488
Samples
Known GenesFSTL5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032161
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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