A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5649n100



Internal ID22791736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:46152326..46389159hg38UCSC Ensembl
chr5:46152428..46389261hg19UCSC Ensembl
chr5:46188185..46425018hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38236834
hg19236834
hg18236834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015614, nsv1028629
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)dgv5649n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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