A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9965n54



Internal ID22777860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99490514..99505551hg38UCSC Ensembl
chr5:98826218..98841255hg19UCSC Ensembl
chr5:98854117..98869154hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3815038
hg1915038
hg1815038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599127, nsv599128
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9965n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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