A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028007



Internal ID18770538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187544955..188590842hg38UCSC Ensembl
Innerchr4:188466109..189511996hg19UCSC Ensembl
Innerchr4:188703103..189748990hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381045888
hg191045888
hg181045888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5496n100
Supporting Variantsnssv3636409
Samples
Known GenesLINC01060, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028007
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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