A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5822n100



Internal ID20157438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155474295..155516009hg38UCSC Ensembl
chr5:154853855..154895569hg19UCSC Ensembl
chr5:154834048..154875762hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3841715
hg1941715
hg1841715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032678, nsv1033393, nsv1019235, nsv1017862
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5822n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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