A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5785n100



Internal ID22791872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114590082..114644459hg38UCSC Ensembl
chr5:113925779..113980156hg19UCSC Ensembl
chr5:113953678..114008055hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3854378
hg1954378
hg1854378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034890, nsv1023944, nsv1015654, nsv1020870
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)dgv5785n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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