A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022237



Internal ID19111455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58017408..58036715hg38UCSC Ensembl
Innerchr5:57313235..57332542hg19UCSC Ensembl
Innerchr5:57348992..57368299hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3819308
hg1919308
hg1819308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5673n100
Supporting Variantsnssv3642171
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)nsv1022237
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