A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033631



Internal ID19122852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131025220..131397019hg38UCSC Ensembl
Innerchr4:131946375..132318174hg19UCSC Ensembl
Innerchr4:132165825..132537624hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38371800
hg19371800
hg18371800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5388n100
Supporting Variantsnssv3639458
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)nsv1033631
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