A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031579



Internal ID19120801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157307369..157484773hg38UCSC Ensembl
Innerchr4:158228521..158405925hg19UCSC Ensembl
Innerchr4:158447971..158625375hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38177405
hg19177405
hg18177405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636148
Samples
Known GenesGRIA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031579
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