A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026047



Internal ID19115264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163314374..163381222hg38UCSC Ensembl
Innerchr5:162741380..162808228hg19UCSC Ensembl
Innerchr5:162673958..162740806hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3866849
hg1966849
hg1866849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5826n100
Supporting Variantsnssv3648236
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)nsv1026047
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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