A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018046



Internal ID19107263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29785669..29818289hg38UCSC Ensembl
Innerchr5:29785776..29818396hg19UCSC Ensembl
Innerchr5:29821533..29854153hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3832621
hg1932621
hg1832621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5615n100
Supporting Variantsnssv3636014
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)nsv1018046
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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