A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5667n100



Internal ID22791754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53311906..53345156hg38UCSC Ensembl
chr5:52607736..52640986hg19UCSC Ensembl
chr5:52643493..52676743hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3833251
hg1933251
hg1833251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016368, nsv1020388
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)dgv5667n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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