A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021013



Internal ID19110231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17045107..17072404hg38UCSC Ensembl
Innerchr9:17045105..17072402hg19UCSC Ensembl
Innerchr9:17035105..17062402hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3827298
hg1927298
hg1827298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7465n100
Supporting Variantsnssv3690643
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)nsv1021013
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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