A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031216



Internal ID19120437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101375798..101396319hg38UCSC Ensembl
Innerchr8:102388026..102408547hg19UCSC Ensembl
Innerchr8:102457202..102477723hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3820522
hg1920522
hg1820522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7276n100
Supporting Variantsnssv3691249
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)nsv1031216
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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