A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018202



Internal ID19107419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83631699..83846576hg38UCSC Ensembl
Innerchr8:84543934..84758811hg19UCSC Ensembl
Innerchr8:84706489..84921366hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38214878
hg19214878
hg18214878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7249n100
Supporting Variantsnssv3689605
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)nsv1018202
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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