A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024069



Internal ID19113286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14345393..15072906hg38UCSC Ensembl
Innerchr8:14202902..14930415hg19UCSC Ensembl
Innerchr8:14247273..14974786hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38727514
hg19727514
hg18727514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675868, nssv3675867
Samples
Known GenesMIR383, SGCZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024069
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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