A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011113



Internal ID19100330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58781791..59397311hg38UCSC Ensembl
Innerchr4:59647956..60263029hg19UCSC Ensembl
Innerchr4:59342713..59945624hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38615521
hg19615074
hg18602912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626505
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)nsv1011113
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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