A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021027



Internal ID19110245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101371556..101396068hg38UCSC Ensembl
Innerchr8:102383784..102408296hg19UCSC Ensembl
Innerchr8:102452960..102477472hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3824513
hg1924513
hg1824513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7276n100
Supporting Variantsnssv3689750
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)nsv1021027
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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