A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5716n100



Internal ID22791803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92855986..93079405hg38UCSC Ensembl
chr5:92191693..92415111hg19UCSC Ensembl
chr5:92217449..92440867hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38223420
hg19223419
hg18223419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028930, nsv1022712
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)dgv5716n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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