A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025989



Internal ID18768521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20971901..21008327hg38UCSC Ensembl
Innerchr8:20829412..20865838hg19UCSC Ensembl
Innerchr8:20873692..20910118hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3836427
hg1936427
hg1836427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760480
Samples
Known GenesLOC286114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025989
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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