A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021629



Internal ID19110847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82115265..82144481hg38UCSC Ensembl
Innerchr8:83027500..83056716hg19UCSC Ensembl
Innerchr8:83190055..83219271hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3829217
hg1929217
hg1829217
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689590
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)nsv1021629
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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