A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691271



Internal ID18989552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:108465005..108489177hg38UCSC Ensembl
Innerchr8:109477234..109501406hg19UCSC Ensembl
Innerchr8:109546410..109570582hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3824173
hg1924173
hg1824173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029325
Supporting Variants
Samples
Known GenesEMC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691271
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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