A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675866



Internal ID18974147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14336731..14429043hg38UCSC Ensembl
Innerchr8:14194240..14286552hg19UCSC Ensembl
Innerchr8:14238611..14330923hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3892313
hg1992313
hg1892313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019053
Supporting Variants
Samples
Known GenesSGCZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3675866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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