A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034158



Internal ID19123380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108659808..108682694hg38UCSC Ensembl
Innerchr5:107995509..108018395hg19UCSC Ensembl
Innerchr5:108023408..108046294hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3822887
hg1922887
hg1822887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647004
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)nsv1034158
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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