A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024150



Internal ID19113367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83575511..83611897hg38UCSC Ensembl
Innerchr8:84487746..84524132hg19UCSC Ensembl
Innerchr8:84650301..84686687hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3836387
hg1936387
hg1836387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7248n100
Supporting Variantsnssv3689602
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)nsv1024150
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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