A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025254



Internal ID19114472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101371556..101390702hg38UCSC Ensembl
Innerchr8:102383784..102402930hg19UCSC Ensembl
Innerchr8:102452960..102472106hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3819147
hg1919147
hg1819147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7276n100
Supporting Variantsnssv3689749, nssv3689748
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)nsv1025254
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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