A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029685



Internal ID19118904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:89909931..89945661hg38UCSC Ensembl
Innerchr5:89205748..89241478hg19UCSC Ensembl
Innerchr5:89241504..89277234hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3835731
hg1935731
hg1835731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5714n100
Supporting Variantsnssv3639185
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)nsv1029685
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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