A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10124n54



Internal ID20143548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151410812..151414457hg38UCSC Ensembl
chr5:150790373..150794018hg19UCSC Ensembl
chr5:150770566..150774211hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383646
hg193646
hg183646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600023, nsv600015, nsv600026
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10124n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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