A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027852



Internal ID18770383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161000260..162322451hg38UCSC Ensembl
Innerchr4:161921412..163243603hg19UCSC Ensembl
Innerchr4:162140862..163463053hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg381322192
hg191322192
hg181322192
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5454n100
Supporting Variantsnssv3634006
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)nsv1027852
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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