A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007909



Internal ID18750440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46750043..46808087hg38UCSC Ensembl
Innerchr3:46791533..46849577hg19UCSC Ensembl
Innerchr3:46766537..46824581hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3858045
hg1958045
hg1858045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4730n100
Supporting Variantsnssv3590909, nssv3590914, nssv3590911, nssv3590913, nssv3590916, nssv3739710, nssv3590910, nssv3590908, nssv3739711, nssv3739709, nssv3590912, nssv3590915
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)nsv1007909
Frequency
Sample Size29084
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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