A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5784n100



Internal ID22791871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113744870..113849664hg38UCSC Ensembl
chr5:113080567..113185361hg19UCSC Ensembl
chr5:113108466..113213260hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38104795
hg19104795
hg18104795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018938, nsv1027940
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)dgv5784n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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