A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689693



Internal ID18987974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88807244..88865957hg38UCSC Ensembl
Innerchr8:89819473..89878186hg19UCSC Ensembl
Innerchr8:89888589..89947302hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3858714
hg1958714
hg1858714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016720
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)nssv3689693
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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