A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021879



Internal ID19111097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:118050382..118234758hg38UCSC Ensembl
Innerchr5:117386077..117570453hg19UCSC Ensembl
Innerchr5:117413976..117598352hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38184377
hg19184377
hg18184377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647223
Samples
Known GenesLOC102467224
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021879
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