A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028046



Internal ID19117264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:24778255..24790740hg38UCSC Ensembl
Innerchr5:24778364..24790849hg19UCSC Ensembl
Innerchr5:24814121..24826606hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3812486
hg1912486
hg1812486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5606n100
Supporting Variantsnssv3635952
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)nsv1028046
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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