A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016862



Internal ID19106079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25400493..25430433hg38UCSC Ensembl
Innerchr5:25400602..25430542hg19UCSC Ensembl
Innerchr5:25436359..25466299hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3829941
hg1929941
hg1829941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5607n100
Supporting Variantsnssv3745859
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)nsv1016862
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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