A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689689



Internal ID18987970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88514342..88597422hg38UCSC Ensembl
Innerchr8:89526571..89609651hg19UCSC Ensembl
Innerchr8:89595687..89678767hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3883081
hg1983081
hg1883081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027744
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)nssv3689689
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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