A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689746



Internal ID18988027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100879617..100908496hg38UCSC Ensembl
Innerchr8:101891845..101920724hg19UCSC Ensembl
Innerchr8:101961021..101989900hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3828880
hg1928880
hg1828880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019998
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)nssv3689746
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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