A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020390



Internal ID19109609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:129373196..129445399hg38UCSC Ensembl
Innerchr5:128708889..128781092hg19UCSC Ensembl
Innerchr5:128736788..128808991hg18UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3872204
hg1972204
hg1872204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648104
Samples
Known GenesMIR4460
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020390
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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