A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022909



Internal ID19112126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32820974..32864164hg38UCSC Ensembl
Innerchr8:32678492..32721682hg19UCSC Ensembl
Innerchr8:32798034..32841224hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3843191
hg1943191
hg1843191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685559
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)nsv1022909
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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