A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026823



Internal ID19116041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14251577..14324341hg38UCSC Ensembl
Innerchr8:14109086..14181850hg19UCSC Ensembl
Innerchr8:14153457..14226221hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3872765
hg1972765
hg1872765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675858
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)nsv1026823
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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