A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028113



Internal ID19117331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13307704..13340012hg38UCSC Ensembl
Innerchr9:13307703..13340011hg19UCSC Ensembl
Innerchr9:13297703..13330011hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3832309
hg1932309
hg1832309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7458n100
Supporting Variantsnssv3690604
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)nsv1028113
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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