A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006809



Internal ID19096027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21754716..21767774hg38UCSC Ensembl
Innerchr3:21796208..21809266hg19UCSC Ensembl
Innerchr3:21771212..21784270hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3813059
hg1913059
hg1813059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4692n100
Supporting Variantsnssv3593157
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)nsv1006809
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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