A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6459n54



Internal ID22774354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42045782..42049652hg38UCSC Ensembl
chr19:42549934..42553804hg19UCSC Ensembl
chr19:47241774..47245644hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383871
hg193871
hg183871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579628, nsv579627
Samples
Known GenesGRIK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6459n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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