A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008527



Internal ID18751058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2956087..3017315hg38UCSC Ensembl
Innerchr4:2957814..3019042hg19UCSC Ensembl
Innerchr4:2927612..2988840hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3861229
hg1961229
hg1861229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5082n100
Supporting Variantsnssv3738105
Samples
Known GenesGRK4, NOP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008527
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