A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015619



Internal ID18758153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186521299..186673904hg38UCSC Ensembl
Innerchr4:187442453..187595058hg19UCSC Ensembl
Innerchr4:187679447..187832052hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38152606
hg19152606
hg18152606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635639
Samples
Known GenesFAT1, MTNR1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015619
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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