A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062709



Internal ID18805240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4653824..4842878hg38UCSC Ensembl
Innerchr19:4653836..4842890hg19UCSC Ensembl
Innerchr19:4604836..4793890hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38189055
hg19189055
hg18189055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564606
Samples
Known GenesC19orf10, DPP9, FEM1A, LOC100131094, MIR7-3, MIR7-3HG, PLIN3, TICAM1, TNFAIP8L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062709
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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