A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689701



Internal ID18987982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89546706..89710352hg38UCSC Ensembl
Innerchr8:90558935..90722580hg19UCSC Ensembl
Innerchr8:90628051..90791702hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38163647
hg19163646
hg18163652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026523
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)nssv3689701
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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