A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032678



Internal ID18775212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:155479846..155510105hg38UCSC Ensembl
Innerchr5:154859406..154889665hg19UCSC Ensembl
Innerchr5:154839599..154869858hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3830260
hg1930260
hg1830260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5822n100
Supporting Variantsnssv3648206
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)nsv1032678
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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