A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675864



Internal ID18974145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14336610..14428799hg38UCSC Ensembl
Innerchr8:14194119..14286308hg19UCSC Ensembl
Innerchr8:14238490..14330679hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3892190
hg1992190
hg1892190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022322
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)nssv3675864
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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