A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002090



Internal ID19091307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166460712..166965620hg38UCSC Ensembl
Innerchr3:166178500..166683408hg19UCSC Ensembl
Innerchr3:167661194..168166102hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38504909
hg19504909
hg18504909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3612694
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)nsv1002090
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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