A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008160



Internal ID19097379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28095766..28115347hg38UCSC Ensembl
Innerchr4:28097388..28116969hg19UCSC Ensembl
Innerchr4:27706486..27726067hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3819582
hg1919582
hg1819582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620619
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)nsv1008160
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