A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3521n100



Internal ID19013889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35358395..35379534hg38UCSC Ensembl
chr19:35849297..35870436hg19UCSC Ensembl
chr19:40541137..40562276hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3821140
hg1921140
hg1821140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056941, nsv1064326, nsv1062973, nsv1059683, nsv1066451, nsv1064284
Samples
Known GenesFFAR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3521n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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