A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997980



Internal ID19157517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3921369..4031048hg38UCSC Ensembl
Innerchr4:3923096..4032775hg19UCSC Ensembl
Innerchr4:3974022..4083676hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38109680
hg19109680
hg18109655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616162
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)nsv997980
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer