A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000809



Internal ID19090026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:76784524..76847016hg38UCSC Ensembl
Innerchr3:76833675..76896167hg19UCSC Ensembl
Innerchr3:76916365..76978857hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3862493
hg1962493
hg1862493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596208
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)nsv1000809
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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