A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022883



Internal ID19112100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25390354..25428595hg38UCSC Ensembl
Innerchr5:25390463..25428704hg19UCSC Ensembl
Innerchr5:25426220..25464461hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3838242
hg1938242
hg1838242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5607n100
Supporting Variantsnssv3745857, nssv3745858, nssv3745855, nssv3745856
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)nsv1022883
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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