A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020859



Internal ID19110077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39999828..40020378hg38UCSC Ensembl
Innerchr8:39857347..39877897hg19UCSC Ensembl
Innerchr8:39976504..39997054hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3820551
hg1920551
hg1820551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687209
Samples
Known GenesIDO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020859
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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