A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019150



Internal ID19108368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164584433..164986772hg38UCSC Ensembl
Innerchr4:165505585..165907924hg19UCSC Ensembl
Innerchr4:165725035..166127374hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38402340
hg19402340
hg18402340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634169
Samples
Known GenesFAM218A, LOC100505989, LOC100506013, MIR5684, TRIM61
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019150
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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