A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056200



Internal ID18798731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1107036..1193347hg38UCSC Ensembl
Innerchr19:1107035..1193346hg19UCSC Ensembl
Innerchr19:1058035..1144346hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3886312
hg1986312
hg1886312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564600
Samples
Known GenesSBNO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056200
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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