A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691249



Internal ID18989530
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 StatusS
Merged Variantsnsv1031216
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)nssv3691249
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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