A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066699



Internal ID18809230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27782693hg38UCSC Ensembl
Innerchr19:27747981..28273601hg19UCSC Ensembl
Innerchr19:32439821..32965441hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38525621
hg19525621
hg18525621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3500n100
Supporting Variantsnssv3724337
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)nsv1066699
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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