A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681736



Internal ID18980017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11544280..11609236hg38UCSC Ensembl
Innerchr8:11401789..11466745hg19UCSC Ensembl
Innerchr8:11439198..11504154hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3864957
hg1964957
hg1864957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033629
Supporting Variants
Samples
Known GenesBLK, LINC00208
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681736
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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