A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028569



Internal ID19117787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131825493..131887539hg38UCSC Ensembl
Innerchr5:131161186..131223232hg19UCSC Ensembl
Innerchr5:131189085..131251131hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3862047
hg1962047
hg1862047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648114
Samples
Known GenesLOC728637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028569
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