A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019424



Internal ID19108642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17049322..17081685hg38UCSC Ensembl
Innerchr9:17049320..17081683hg19UCSC Ensembl
Innerchr9:17039320..17071683hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3832364
hg1932364
hg1832364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7465n100
Supporting Variantsnssv3690645
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)nsv1019424
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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