A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024390



Internal ID18766922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:375290..438449hg38UCSC Ensembl
Innerchr5:375405..438564hg19UCSC Ensembl
Innerchr5:428405..491564hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3863160
hg1963160
hg1863160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5520n100
Supporting Variantsnssv3633219
Samples
Known GenesAHRR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024390
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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