A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015939



Internal ID19105157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186467804..186533466hg38UCSC Ensembl
Innerchr4:187388958..187454620hg19UCSC Ensembl
Innerchr4:187625952..187691614hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3865663
hg1965663
hg1865663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635636
Samples
Known GenesF11-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015939
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