A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9767n54



Internal ID22777662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:50110886..50145767hg38UCSC Ensembl
chr5:49406720..49441601hg19UCSC Ensembl
chr5:49442477..49477358hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3834882
hg1934882
hg1834882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv598085, nsv598086, nsv598087
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9767n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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