A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021225



Internal ID19110443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19697349..19729069hg38UCSC Ensembl
Innerchr8:19554860..19586580hg19UCSC Ensembl
Innerchr8:19599140..19630860hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3831721
hg1931721
hg1831721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685329
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)nsv1021225
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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