A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001364



Internal ID19090581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:84271901..84331168hg38UCSC Ensembl
Innerchr4:85193054..85252321hg19UCSC Ensembl
Innerchr4:85412078..85471345hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3859268
hg1959268
hg1859268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5331n100
Supporting Variantsnssv3633901
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001364
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