A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063469



Internal ID18806000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:310162..384644hg38UCSC Ensembl
Innerchr19:310162..384644hg19UCSC Ensembl
Innerchr19:261162..335644hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3874483
hg1974483
hg1874483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3420n100
Supporting Variantsnssv3564596
Samples
Known GenesMIER2, THEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063469
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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