A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066032



Internal ID19155251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27590467hg38UCSC Ensembl
Innerchr19:27747981..28081375hg19UCSC Ensembl
Innerchr19:32439821..32773215hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38333395
hg19333395
hg18333395
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3498n100
Supporting Variantsnssv3572022, nssv3572023, nssv3572024
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)nsv1066032
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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