A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028974



Internal ID19118193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152134260..152144649hg38UCSC Ensembl
Innerchr5:151513821..151524210hg19UCSC Ensembl
Innerchr5:151494014..151504403hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3810390
hg1910390
hg1810390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5819n100
Supporting Variantsnssv3648182, nssv3648181
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)nsv1028974
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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