A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015850



Internal ID19105068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57295967..57340222hg38UCSC Ensembl
Innerchr8:58208526..58252781hg19UCSC Ensembl
Innerchr8:58371080..58415335hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3844256
hg1944256
hg1844256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689448, nssv3757279
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)nsv1015850
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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