A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065696



Internal ID19154915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27550910hg38UCSC Ensembl
Innerchr19:27747981..28041818hg19UCSC Ensembl
Innerchr19:32439821..32733658hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38293838
hg19293838
hg18293838
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3498n100
Supporting Variantsnssv3571999, nssv3572005, nssv3572002, nssv3572003, nssv3571995, nssv3571994, nssv3572008, nssv3572006, nssv3572007, nssv3571990, nssv3572000, nssv3571992, nssv3571991, nssv3572004, nssv3571996, nssv3571997, nssv3572001, nssv3571998, nssv3571993
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)nsv1065696
Frequency
Sample Size11257
Observed Gain13
Observed Loss6
Observed Complex0
Frequencyn/a


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