A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061063



Internal ID19150282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27294573hg38UCSC Ensembl
Innerchr19:27747981..27785481hg19UCSC Ensembl
Innerchr19:32439821..32477321hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3837501
hg1937501
hg1837501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3493n100
Supporting Variantsnssv3570790
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)nsv1061063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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