A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017726



Internal ID19106943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121295259..121327482hg38UCSC Ensembl
Innerchr8:122307499..122339722hg19UCSC Ensembl
Innerchr8:122376680..122408903hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3832224
hg1932224
hg1832224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691474
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)nsv1017726
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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