A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6416n54



Internal ID18998592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35268140..35270013hg38UCSC Ensembl
chr19:35759043..35760916hg19UCSC Ensembl
chr19:40450883..40452756hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381874
hg191874
hg181874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579391, nsv579390
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6416n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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