A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024584



Internal ID19113801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:48966578..48994221hg38UCSC Ensembl
Innerchr8:49879137..49906780hg19UCSC Ensembl
Innerchr8:50041690..50069333hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3827644
hg1927644
hg1827644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687465
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)nsv1024584
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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