A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019390



Internal ID19108608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131591556..131629260hg38UCSC Ensembl
Innerchr4:132512711..132550415hg19UCSC Ensembl
Innerchr4:132732161..132769865hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3837705
hg1937705
hg1837705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5391n100
Supporting Variantsnssv3639491, nssv3639489, nssv3639490
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)nsv1019390
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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