A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691248



Internal ID18989529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101375798..101396068hg38UCSC Ensembl
Innerchr8:102388026..102408296hg19UCSC Ensembl
Innerchr8:102457202..102477472hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3820271
hg1920271
hg1820271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021737
Supporting Variants
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)nssv3691248
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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