A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689463



Internal ID18987744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60076865..60095198hg38UCSC Ensembl
Innerchr8:60989424..61007757hg19UCSC Ensembl
Innerchr8:61151978..61170311hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3818334
hg1918334
hg1818334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015316
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)nssv3689463
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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