A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049034



Internal ID19138253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123967180..123988966hg38UCSC Ensembl
Innerchr9:126729459..126751245hg19UCSC Ensembl
Innerchr9:125769280..125791066hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3821787
hg1921787
hg1821787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759824
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)nsv1049034
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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