A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025083



Internal ID19114301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20425499..20444181hg38UCSC Ensembl
Innerchr5:20425608..20444290hg19UCSC Ensembl
Innerchr5:20461365..20480047hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3818683
hg1918683
hg1818683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635919
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)nsv1025083
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